ID

22539

Beschrijving

PROFIT - Prostate Fractionated Irradiation Trial; ODM derived from: https://clinicaltrials.gov/show/NCT00304759

Link

https://clinicaltrials.gov/show/NCT00304759

Trefwoorden

Versies (1)
  1. 07-06-17 07-06-17 -
Geüploaded op

7 juni 2017

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Prostate Cancer NCT00304759

Engels

Eligibility Prostate Cancer NCT00304759

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. histologic diagnosis of carcinoma of the prostate within 6 months of entry without evidence of metastatic disease to the lymph nodes, bone or lung;
Beschrijving

Prostate carcinoma | Secondary malignant neoplasm of lymph node Absent | Secondary malignant neoplasm of bone Absent | Secondary malignant neoplasm of lung Absent

Datatype

boolean

Alias
UMLS CUI [1]
C0600139
UMLS CUI [2,1]
C0686619
UMLS CUI [2,2]
C0332197
UMLS CUI [3,1]
C0153690
UMLS CUI [3,2]
C0332197
UMLS CUI [4,1]
C0153676
UMLS CUI [4,2]
C0332197
2. intermediate risk prostate cancer (that is, t1-2a, gleason score <6, psa 10.1-20.0 ng/ml; t2b-c gleason <6, psa ≤ 20.0 ng/ml; t1-2, gleason 7, psa ≤ 20.0 ng/ml).
Beschrijving

Intermediate Risk Prostate carcinoma | TNM clinical staging | Gleason score | Prostate specific antigen measurement

Datatype

boolean

Alias
UMLS CUI [1,1]
C3640764
UMLS CUI [1,2]
C0600139
UMLS CUI [2]
C3258246
UMLS CUI [3]
C3203027
UMLS CUI [4]
C0201544
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. histologic diagnosis of carcinoma of the prostate more than six months prior to study entry;
Beschrijving

Prostate carcinoma Disease length

Datatype

boolean

Alias
UMLS CUI [1,1]
C0600139
UMLS CUI [1,2]
C0872146
2. previous therapy for carcinoma of the prostate other than biopsy or transurethral resection;
Beschrijving

Therapeutic procedure Prostate carcinoma | Biopsy of prostate | Transurethral Resection

Datatype

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0600139
UMLS CUI [2]
C0194804
UMLS CUI [3]
C1519630
3. patients previously on more than 12 weeks of hormone therapy for treatment of their prostate cancer;
Beschrijving

Hormone Therapy Prostate carcinoma

Datatype

boolean

Alias
UMLS CUI [1,1]
C0279025
UMLS CUI [1,2]
C0600139
4. any other active malignancy (untreated, progressive or recurrent), except for non-melanoma skin cancer. any inactive malignancy diagnosed within 5 years of entry, except for non-melanoma skin cancer;
Beschrijving

Malignant Neoplasm Untreated | Malignant Neoplasm Progressive | Recurrent tumor | Skin carcinoma | Malignant Neoplasm inactive

Datatype

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0332155
UMLS CUI [2,1]
C0006826
UMLS CUI [2,2]
C0205329
UMLS CUI [3]
C0521158
UMLS CUI [4]
C0699893
UMLS CUI [5,1]
C0006826
UMLS CUI [5,2]
C0544452
5. treatment plan cannot meet dose constraints for the hypofractionation arm of the trial;
Beschrijving

Treatment Plan Inconsistent Dose Hypofractionation Constraint

Datatype

boolean

Alias
UMLS CUI [1,1]
C0599880
UMLS CUI [1,2]
C0442809
UMLS CUI [1,3]
C4042795
UMLS CUI [1,4]
C0443288
6. previous pelvic radiotherapy;
Beschrijving

Radiotherapy to pelvis

Datatype

boolean

Alias
UMLS CUI [1]
C1536155
7. inflammatory bowel disease.
Beschrijving

Inflammatory Bowel Diseases

Datatype

boolean

Alias
UMLS CUI [1]
C0021390
Terug naar het begin van de pagina

Similar models

Eligibility Prostate Cancer NCT00304759

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Prostate carcinoma | Secondary malignant neoplasm of lymph node Absent | Secondary malignant neoplasm of bone Absent | Secondary malignant neoplasm of lung Absent
Item
1. histologic diagnosis of carcinoma of the prostate within 6 months of entry without evidence of metastatic disease to the lymph nodes, bone or lung;
boolean
C0600139 (UMLS CUI [1])
C0686619 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0153690 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0153676 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
Intermediate Risk Prostate carcinoma | TNM clinical staging | Gleason score | Prostate specific antigen measurement
Item
2. intermediate risk prostate cancer (that is, t1-2a, gleason score <6, psa 10.1-20.0 ng/ml; t2b-c gleason <6, psa ≤ 20.0 ng/ml; t1-2, gleason 7, psa ≤ 20.0 ng/ml).
boolean
C3640764 (UMLS CUI [1,1])
C0600139 (UMLS CUI [1,2])
C3258246 (UMLS CUI [2])
C3203027 (UMLS CUI [3])
C0201544 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
Prostate carcinoma Disease length
Item
1. histologic diagnosis of carcinoma of the prostate more than six months prior to study entry;
boolean
C0600139 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
Therapeutic procedure Prostate carcinoma | Biopsy of prostate | Transurethral Resection
Item
2. previous therapy for carcinoma of the prostate other than biopsy or transurethral resection;
boolean
C0087111 (UMLS CUI [1,1])
C0600139 (UMLS CUI [1,2])
C0194804 (UMLS CUI [2])
C1519630 (UMLS CUI [3])
Hormone Therapy Prostate carcinoma
Item
3. patients previously on more than 12 weeks of hormone therapy for treatment of their prostate cancer;
boolean
C0279025 (UMLS CUI [1,1])
C0600139 (UMLS CUI [1,2])
Malignant Neoplasm Untreated | Malignant Neoplasm Progressive | Recurrent tumor | Skin carcinoma | Malignant Neoplasm inactive
Item
4. any other active malignancy (untreated, progressive or recurrent), except for non-melanoma skin cancer. any inactive malignancy diagnosed within 5 years of entry, except for non-melanoma skin cancer;
boolean
C0006826 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
C0006826 (UMLS CUI [2,1])
C0205329 (UMLS CUI [2,2])
C0521158 (UMLS CUI [3])
C0699893 (UMLS CUI [4])
C0006826 (UMLS CUI [5,1])
C0544452 (UMLS CUI [5,2])
Treatment Plan Inconsistent Dose Hypofractionation Constraint
Item
5. treatment plan cannot meet dose constraints for the hypofractionation arm of the trial;
boolean
C0599880 (UMLS CUI [1,1])
C0442809 (UMLS CUI [1,2])
C4042795 (UMLS CUI [1,3])
C0443288 (UMLS CUI [1,4])
Radiotherapy to pelvis
Item
6. previous pelvic radiotherapy;
boolean
C1536155 (UMLS CUI [1])
Inflammatory Bowel Diseases
Item
7. inflammatory bowel disease.
boolean
C0021390 (UMLS CUI [1])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial