ID

27670

Description

Study ID: 103094 Clinical Study ID: ARI103094 Study Title: ARI103094-Follow-Up Study for REDUCE Study Subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00883909 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: dutasteride Trade Name: Zytefor,Zyfetor,Duagen,Avolve,Avodart,Avidart Study Indication: Neoplasms, Prostate CRF Seiten: 934-977

Mots-clés

Versions (2)
  1. 09/11/2017 09/11/2017 -
  2. 26/11/2017 26/11/2017 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

26 novembre 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
Modèle Commentaires :

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Previous Clinical Trial Participation GSK study Prostatic neoplasms NCT00883909

Anglais

Previous Clinical Trial Participation GSK study Prostatic neoplasms NCT00883909

1 Formulaires  
Administrative data
Description

Administrative data

Alias
UMLS CUI-1
C1320722
Session number
Description

Session number

Type de données

integer

Alias
UMLS CUI [1,1]
C1883017
UMLS CUI [1,2]
C0750480
Subject number
Description

Subject number

Type de données

text

Alias
UMLS CUI [1]
C2348585
Previous Clinical Trial Participation
Description

Previous Clinical Trial Participation

Alias
UMLS CUI-1
C2348568
Date of REDUCE 4 Year Contact
Description

The REDUCE 4 Year Contact is either: a) a REDUCE 4 Year clinic visit for subjects on treatment (Visit 10), or b) a REDUCE 4 Year clinic visit for subjects in Prostate Cancer Follow-Up (Visit 10P), or c) a 4 Year phone call for subjects in Phone Follow-Up

Type de données

date

Alias
UMLS CUI [1]
C1320303
Date Investigational Product Stopped
Description

Date Investigational Product Stopped

Type de données

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0304229
UMLS CUI [1,3]
C0457454
Was the subject previously diagnosed with prostate cancer during the REDUCE (ARI40006) study?
Description

previous diagnosis of prostate cancer

Type de données

text

Alias
UMLS CUI [1,1]
C0332132
UMLS CUI [1,2]
C0600139
If YES, record the date of the biopsy resulting in prostate cancer diagnosis
Description

date of biopsy

Type de données

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0005558
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Similar models

Previous Clinical Trial Participation GSK study Prostatic neoplasms NCT00883909

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Administrative data
C1320722 (UMLS CUI-1)
Session number
Item
Session number
integer
C1883017 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
Subject number
Item
Subject number
text
C2348585 (UMLS CUI [1])
Item Group
Previous Clinical Trial Participation
C2348568 (UMLS CUI-1)
Date of visit
Item
Date of REDUCE 4 Year Contact
date
C1320303 (UMLS CUI [1])
Date Investigational Product Stopped
Item
Date Investigational Product Stopped
date
C0011008 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
C0457454 (UMLS CUI [1,3])
Item
Was the subject previously diagnosed with prostate cancer during the REDUCE (ARI40006) study?
text
C0332132 (UMLS CUI [1,1])
C0600139 (UMLS CUI [1,2])
previous diagnosis of prostate cancer
Code List
Was the subject previously diagnosed with prostate cancer during the REDUCE (ARI40006) study?
CL Item
Yes (Y)
CL Item
No (N)
date of biopsy
Item
If YES, record the date of the biopsy resulting in prostate cancer diagnosis
date
C0011008 (UMLS CUI [1,1])
C0005558 (UMLS CUI [1,2])
Retour au début de la page 

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