ID

27670

Descripción

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

Palabras clave

Versiones (2)
  1. 9/11/17 9/11/17 -
  2. 26/11/17 26/11/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

26 de noviembre de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0
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Previous Clinical Trial Participation GSK study Prostatic neoplasms NCT00883909

Inglés

Previous Clinical Trial Participation GSK study Prostatic neoplasms NCT00883909

1 formularios  
Administrative data
Descripción

Administrative data

Alias
UMLS CUI-1
C1320722
Session number
Descripción

Session number

Tipo de datos

integer

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

Subject number

Tipo de datos

text

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

Previous Clinical Trial Participation

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

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

Tipo de datos

date

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

Date Investigational Product Stopped

Tipo de datos

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?
Descripción

previous diagnosis of prostate cancer

Tipo de datos

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
Descripción

date of biopsy

Tipo de datos

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 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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])
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