Informatie:
Fout:
ID
36887
Beschrijving
Development of a Therapeutic Education Program for Patients Operated for Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02379260
Link
https://clinicaltrials.gov/show/NCT02379260
Trefwoorden
Versies (1)
- 18-06-19 18-06-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
18 juni 2019
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Prostate Cancer NCT02379260
Eligibility Prostate Cancer NCT02379260
- StudyEvent: Eligibility
Similar models
Eligibility Prostate Cancer NCT02379260
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Patients Urology department
Item
patients followed in urology department lyon sud ch:
boolean
C0030705 (UMLS CUI [1,1])
C0587531 (UMLS CUI [1,2])
C0587531 (UMLS CUI [1,2])
Age
Item
aged over 18 year
boolean
C0001779 (UMLS CUI [1])
Prostate carcinoma
Item
having a prostate cancer
boolean
C0600139 (UMLS CUI [1])
Radical prostatectomy | Other Coding
Item
treated with radical prostatectomy with or without conservation strips neuro vascular
boolean
C0194810 (UMLS CUI [1])
C3846158 (UMLS CUI [2])
C3846158 (UMLS CUI [2])
Postoperative Period Duration
Item
more than 1 month postoperative
boolean
C0032790 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
Function Erectile Preoperative IIEF
Item
having a normal preoperative erectile function defined by a score iief ef ≥ 26.
boolean
C0031843 (UMLS CUI [1,1])
C0030847 (UMLS CUI [1,2])
C0445204 (UMLS CUI [1,3])
C3641331 (UMLS CUI [1,4])
C0030847 (UMLS CUI [1,2])
C0445204 (UMLS CUI [1,3])
C3641331 (UMLS CUI [1,4])
Informed Consent
Item
and who signed the informed consent form for participation in the study
boolean
C0021430 (UMLS CUI [1])
Function Erectile Preoperative IIEF
Item
score preoperative iief ef <26
boolean
C0031843 (UMLS CUI [1,1])
C0030847 (UMLS CUI [1,2])
C0445204 (UMLS CUI [1,3])
C3641331 (UMLS CUI [1,4])
C0030847 (UMLS CUI [1,2])
C0445204 (UMLS CUI [1,3])
C3641331 (UMLS CUI [1,4])
Participation Refused | Informed Consent Patients Guardianship
Item
refusal of participation, signed consent major patients protected under guardianship.
boolean
C0679823 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0030705 (UMLS CUI [2,2])
C0870627 (UMLS CUI [2,3])
C1705116 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0030705 (UMLS CUI [2,2])
C0870627 (UMLS CUI [2,3])
Study Protocol Comprehension Unable
Item
patients unable to understand the course of the study
boolean
C2348563 (UMLS CUI [1,1])
C0162340 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0162340 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Cognition Disorders | Mental disorders
Item
patient (s) with a documented history of cognitive or psychiatric disorders.
boolean
C0009241 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
C0004936 (UMLS CUI [2])
Geographic Factor | Residence Remote
Item
geographical remoteness of more than 100 kms.
boolean
C0017444 (UMLS CUI [1])
C0237096 (UMLS CUI [2,1])
C0205157 (UMLS CUI [2,2])
C0237096 (UMLS CUI [2,1])
C0205157 (UMLS CUI [2,2])