ID

36887

Description

Development of a Therapeutic Education Program for Patients Operated for Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02379260

Lien

https://clinicaltrials.gov/show/NCT02379260

Mots-clés

Versions (1)
  1. 18/06/2019 18/06/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

18 juin 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Prostate Cancer NCT02379260

Anglais

Eligibility Prostate Cancer NCT02379260

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients followed in urology department lyon sud ch:
Description

Patients Urology department

Type de données

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0587531
aged over 18 year
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
having a prostate cancer
Description

Prostate carcinoma

Type de données

boolean

Alias
UMLS CUI [1]
C0600139
treated with radical prostatectomy with or without conservation strips neuro vascular
Description

Radical prostatectomy | Other Coding

Type de données

boolean

Alias
UMLS CUI [1]
C0194810
UMLS CUI [2]
C3846158
more than 1 month postoperative
Description

Postoperative Period Duration

Type de données

boolean

Alias
UMLS CUI [1,1]
C0032790
UMLS CUI [1,2]
C0449238
having a normal preoperative erectile function defined by a score iief ef ≥ 26.
Description

Function Erectile Preoperative IIEF

Type de données

boolean

Alias
UMLS CUI [1,1]
C0031843
UMLS CUI [1,2]
C0030847
UMLS CUI [1,3]
C0445204
UMLS CUI [1,4]
C3641331
and who signed the informed consent form for participation in the study
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
score preoperative iief ef <26
Description

Function Erectile Preoperative IIEF

Type de données

boolean

Alias
UMLS CUI [1,1]
C0031843
UMLS CUI [1,2]
C0030847
UMLS CUI [1,3]
C0445204
UMLS CUI [1,4]
C3641331
refusal of participation, signed consent major patients protected under guardianship.
Description

Participation Refused | Informed Consent Patients Guardianship

Type de données

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C1705116
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0030705
UMLS CUI [2,3]
C0870627
patients unable to understand the course of the study
Description

Study Protocol Comprehension Unable

Type de données

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0162340
UMLS CUI [1,3]
C1299582
patient (s) with a documented history of cognitive or psychiatric disorders.
Description

Cognition Disorders | Mental disorders

Type de données

boolean

Alias
UMLS CUI [1]
C0009241
UMLS CUI [2]
C0004936
geographical remoteness of more than 100 kms.
Description

Geographic Factor | Residence Remote

Type de données

boolean

Alias
UMLS CUI [1]
C0017444
UMLS CUI [2,1]
C0237096
UMLS CUI [2,2]
C0205157
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Similar models

Eligibility Prostate Cancer NCT02379260

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Patients Urology department
Item
patients followed in urology department lyon sud ch:
boolean
C0030705 (UMLS CUI [1,1])
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])
Postoperative Period Duration
Item
more than 1 month postoperative
boolean
C0032790 (UMLS CUI [1,1])
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])
Informed Consent
Item
and who signed the informed consent form for participation in the study
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
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])
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])
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])
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])
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])
Retour au début de la page 

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