ID
40563
Descrizione
ADVANCED PROSTATE CANCER DATA COLLECTION Version 2.3.1 Revised: April 10th, 2017 International Consortium for Health Outcomes Measurement (ICHOM), Source: http://www.ichom.org/ Notice: This work was conducted using resources from ICHOM, the International Consortium for Health Outcomes Measurement (www.ICHOM.org). The content is solely the responsibility of the authors and does not necessarily represent the official views of ICHOM. Conditions: All patients with advanced prostate cancer, either having metastatic disease or biochemical recurrence progressing after salvage treatment or ineligible for salvage treatment. Patients with biochemical recurrence treated with salvage therapy are referred to the localized prostate cancer set. Treatment Approaches: Hormonal Therapy | Chemotherapy | Immunotherapy | Radiopharmaceuticals | Radiation | Interventions for Complications of Local Progression This form contains patient-reported variables, to be assessed at baseline. Questionnaires used in this form: Expanded Prostate Cancer Index Composite (EPIC-26): The EPIC-26 is free for all health care organizations, and a license is not needed. The scoring guide may be found at http://www.med.umich.edu/urology/research/EPIC/EPIC-26-Scoring-1.2007.pdf ; Wei J, Dunn R, Litwin M, Sandler H, and Sanda M. "Development and Validation of the Expanded Prostate Cancer Index Composite (EPIC) for Comprehensive Assessment of Health-Related Quality of Life in Men with Prostate Cancer", Urology. 56: 899-905, 2000. For registries choosing to implement the EPIC‐CP rather than the EPIC‐26, we recommend using the same variable IDs as the corresponding EPIC‐26 questions. This means that only questions 2, 3, 4a, 4b, 4d, 4e, 5, 6e, 6b, 7, 8b, 9, 12, 13a, 13c, and 13d of the EPIC-26 are administered. Utilization of Sexual Medications/Devices: The Utilization of Sexual Medications/Devices is free for all health care organizations, and a license is not needed (according to ICHOM). Refer to http://dx.doi.org/10.1016/j.urology.2006.01.077 for more information European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30): For use of the EORTC QLQ-C30 a license is needed, therefore the questions will not be part of this version of the standard set. (eortc.be) The following paper has been published about development of this standard set: Morgans AK, van Bommel ACM, Stowell C, Abrahm JL, Basch E, Bekelman JE, et al. Development of a Standardized Set of Patient-centered Outcomes for Advanced Prostate Cancer: An International Effort for a Unified Approach. Eur Urol. 2015 Nov;68(5):891–8. For the standard set ICHOM has been supported by the Movember Foundation. For this version of the standard set, semantic annotation with UMLS CUIs has been added.
collegamento
Keywords
versioni (4)
- 07/12/17 07/12/17 -
- 29/11/18 29/11/18 - Sarah Riepenhausen
- 29/11/18 29/11/18 - Sarah Riepenhausen
- 30/04/20 30/04/20 - Sarah Riepenhausen
Titolare del copyright
ICHOM
Caricato su
30 aprile 2020
DOI
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Licenza
Creative Commons BY-NC 4.0
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ICHOM Advanced Prostate Cancer
Baseline Patient-reported Form
- StudyEvent: ODM
Descrizione
Demographic factors
Alias
- UMLS CUI-1
- C1704791
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical or patient-reported TYPE: Date by DD/MM/YYYY
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C0421451
Descrizione
Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Numerical value RESPONSE OPTIONS: Numerical value of height in cm or in
Tipo di dati
float
Alias
- UMLS CUI [1]
- C0005890
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0005890
- UMLS CUI [1,2]
- C1519795
Descrizione
Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Numerical value RESPONSE OPTIONS: Numerical value of weight in kg or lbs
Tipo di dati
float
Alias
- UMLS CUI [1]
- C0005910
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0005910
- UMLS CUI [1,2]
- C1519795
Descrizione
Varies by country and should be determined by country (not for cross country comparison). This is based upon the U.S. Standards for the Classification of Federal Data on Race and Ethnicity, and reflects standards in the U.S. Please adapt questions according to your country’s guidelines. INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer (https://ichom.co1.qualtrics.com/jfe/form/SV_8AhYQGQKZE2tRwV?Q_JFE=qdg linked in Reference Guide it is multiple answer)
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C1515945
Descrizione
Varies by country and should be determined by country (not for cross country comparison). This is based upon the U.S. Standards for the Classification of Federal Data on Race and Ethnicity, and reflects standards in the U.S. Please adapt questions according to your country’s guidelines. INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer (https://ichom.co1.qualtrics.com/jfe/form/SV_8AhYQGQKZE2tRwV?Q_JFE=qdg linked in Reference Guide it is multiple answer)
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C0078988
Descrizione
Varies by country and should be determined by country (not for cross country comparison). This is based upon the U.S. Standards for the Classification of Federal Data on Race and Ethnicity, and reflects standards in the U.S. Please adapt questions according to your country’s guidelines. INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer (https://ichom.co1.qualtrics.com/jfe/form/SV_8AhYQGQKZE2tRwV?Q_JFE=qdg linked in Reference Guide it is multiple answer)
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C0005680
- UMLS CUI [2,1]
- C0015031
- UMLS CUI [2,2]
- C0085756
Descrizione
Varies by country and should be determined by country (not for cross country comparison). This is based upon the U.S. Standards for the Classification of Federal Data on Race and Ethnicity, and reflects standards in the U.S. Please adapt questions according to your country’s guidelines. INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer (https://ichom.co1.qualtrics.com/jfe/form/SV_8AhYQGQKZE2tRwV?Q_JFE=qdg linked in Reference Guide it is multiple answer)
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C0086409
- UMLS CUI [2,1]
- C0015031
- UMLS CUI [2,2]
- C0086528
Descrizione
Varies by country and should be determined by country (not for cross country comparison). This is based upon the U.S. Standards for the Classification of Federal Data on Race and Ethnicity, and reflects standards in the U.S. Please adapt questions according to your country’s guidelines. INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer (https://ichom.co1.qualtrics.com/jfe/form/SV_8AhYQGQKZE2tRwV?Q_JFE=qdg linked in Reference Guide it is multiple answer)
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C1513907
Descrizione
Varies by country and should be determined by country (not for cross country comparison). This is based upon the U.S. Standards for the Classification of Federal Data on Race and Ethnicity, and reflects standards in the U.S. Please adapt questions according to your country’s guidelines. INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer (https://ichom.co1.qualtrics.com/jfe/form/SV_8AhYQGQKZE2tRwV?Q_JFE=qdg linked in Reference Guide it is multiple answer)
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C0007457
Descrizione
The level of schooling is defined in each country as per ISCED [International Standard Classification] INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0013658
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0024819
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C2184149
Descrizione
Baseline Clinical Factors
Alias
- UMLS CUI-1
- C0449440
- UMLS CUI-2
- C1442488
Descrizione
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Multiple answer (Separate multiple entries with "";"")
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0549184
Descrizione
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Multiple answer (Separate multiple entries with "";"")
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0018799
Descrizione
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Multiple answer (Separate multiple entries with "";"")
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0020538
Descrizione
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Multiple answer (Separate multiple entries with "";"")
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0085096
- UMLS CUI [1,2]
- C0009488
Descrizione
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Multiple answer (Separate multiple entries with "";"")
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0024115
Descrizione
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Multiple answer (Separate multiple entries with "";"")
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0011849
Descrizione
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Multiple answer (Separate multiple entries with "";"")
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0022658
Descrizione
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Multiple answer (Separate multiple entries with "";"")
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0023895
Descrizione
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Multiple answer (Separate multiple entries with "";"")
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0038454
Descrizione
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Multiple answer (Separate multiple entries with "";"")
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0027765
Descrizione
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Multiple answer (Separate multiple entries with "";"")
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C1707251
Descrizione
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Multiple answer (Separate multiple entries with "";"")
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0011581
Descrizione
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Multiple answer (Separate multiple entries with "";"")
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0003864
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Numerical value RESPONSE OPTIONS: Ordinal values from 0 to 10, with 'No pain' marked at '0' and 'Worst pain imaginable' marked at '10'
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0582148
Descrizione
A first degree relative is a father, brother, or son INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C1532320
Descrizione
Degree of health
Alias
- UMLS CUI-1
- C0018759
Descrizione
Over the counter pain medicine is for example paracetamol, NSAIDS INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Multiple answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0002771
- UMLS CUI [1,2]
- C1298908
Descrizione
Over the counter pain medicine is for example paracetamol, NSAIDS INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Multiple answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0002771
- UMLS CUI [1,2]
- C0013231
- UMLS CUI [2,1]
- C0002771
- UMLS CUI [2,2]
- C2709201
Descrizione
Over the counter pain medicine is for example paracetamol, NSAIDS INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Multiple answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0002771
- UMLS CUI [1,2]
- C0304227
- UMLS CUI [2]
- C0027409
- UMLS CUI [3]
- C0002772
Descrizione
As a license is needed for use of this questionnaire, the 30 actual questions are not included in this version of the standard set. ICHOM IDs are EORTCQLQC30_Q01 up to EORTCQLQC30_Q30. INCLUSION CRITERIA: All patients TIMING: Baseline, 30 days + annually up to 5 years after index event REPORTING SOURCE: Patient-reported TYPE: Numerical (each question is single answer in original set)
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C4055104
- UMLS CUI [1,2]
- C2964552
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289637
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289645
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289630
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289641
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289629
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289644
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289625
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289626
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289631
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289627
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289636
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289634
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4287870
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289649
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289633
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289647
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289646
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289628
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289639
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289648
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289632
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289638
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289643
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289640
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289635
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289642
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3899191
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3827672
Descrizione
INCLUSION CRITERIA: All patients, If answered 'yes' to using medications or devices to aid or improve erections (LIBID_Q02) TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0663448
Descrizione
INCLUSION CRITERIA: All patients, If answered 'yes' to using medications or devices to aid or improve erections (LIBID_Q02) TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C2366566
Descrizione
INCLUSION CRITERIA: All patients, If answered 'yes' to using medications or devices to aid or improve erections (LIBID_Q02) TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3828613
Descrizione
INCLUSION CRITERIA: All patients, If answered 'yes' to using medications or devices to aid or improve erections (LIBID_Q02) TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3827672
Descrizione
INCLUSION CRITERIA: All patients, If answered 'yes' to using medications or devices to aid or improve erections (LIBID_Q02) TIMING: Baseline, 3 months post initiation of treatment, 6 months post initiation of treatment, 1 year post initiation of treatment, Tracked ongoing annually for life REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C1115771
Similar models
Baseline Patient-reported Form
- StudyEvent: ODM
C1519795 (UMLS CUI [1,2])
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C1519795 (UMLS CUI [1,2])
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C1515945 (UMLS CUI [1,2])
C0078988 (UMLS CUI [1,2])
C0005680 (UMLS CUI [1,2])
C0015031 (UMLS CUI [2,1])
C0085756 (UMLS CUI [2,2])
C0086409 (UMLS CUI [1,2])
C0015031 (UMLS CUI [2,1])
C0086528 (UMLS CUI [2,2])
C1513907 (UMLS CUI [1,2])
C0007457 (UMLS CUI [1,2])
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C0033145 (UMLS CUI-2)
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C1546497 (UMLS CUI-2)
C2003901 (UMLS CUI-3)
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C0682323 (UMLS CUI-2)
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C2184147 (UMLS CUI-2)
C0557130 (UMLS CUI-3)
C0557128 (UMLS CUI-4)
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C0557218 (UMLS CUI-2)
C3640869 (UMLS CUI-3)
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C0237096 (UMLS CUI-2)
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C1442488 (UMLS CUI-2)
C0549184 (UMLS CUI [1,2])
C0018799 (UMLS CUI [1,2])
C0020538 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,2])
C0024115 (UMLS CUI [1,2])
C0011849 (UMLS CUI [1,2])
C0022658 (UMLS CUI [1,2])
C0023895 (UMLS CUI [1,2])
C0038454 (UMLS CUI [1,2])
C0027765 (UMLS CUI [1,2])
C1707251 (UMLS CUI [1,2])
C0011581 (UMLS CUI [1,2])
C0003864 (UMLS CUI [1,2])
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C1298908 (UMLS CUI [1,2])
C0013231 (UMLS CUI [1,2])
C0002771 (UMLS CUI [2,1])
C2709201 (UMLS CUI [2,2])
C0304227 (UMLS CUI [1,2])
C0027409 (UMLS CUI [2])
C0002772 (UMLS CUI [3])
C2964552 (UMLS CUI [1,2])
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C0558293 (UMLS CUI-2)
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C2003901 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0549184 (UMLS CUI-2)
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C0549184 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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C0442811 (UMLS CUI-2)
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C0700321 (UMLS CUI-2)
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C0205081 (UMLS CUI-2)
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C1298908 (UMLS CUI-2)
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C0549177 (UMLS CUI-2)
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