ID

27362

Beschrijving

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

Trefwoorden

Versies (2)
  1. 09-11-17 09-11-17 -
  2. 26-11-17 26-11-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

9 november 2017

DOI

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Licentie

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

Engels

Previous Clinical Trial Participation GSK study Prostatic neoplasms NCT00883909

1 Formulieren  
Administrative data
Beschrijving

Administrative data

Session number
Beschrijving

Session number

Datatype

integer

Subject number
Beschrijving

Subject number

Datatype

text

Previous Clinical Trial Participation
Beschrijving

Previous Clinical Trial Participation

Date of REDUCE 4 Year Contact
Beschrijving

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

Datatype

date

Date Investigational Product Stopped
Beschrijving

Date Investigational Product Stopped

Datatype

date

Was the subject previously diagnosed with prostate cancer during the REDUCE (ARI40006) study?
Beschrijving

previous diagnosis of prostate cancer

Datatype

text

If YES, record the date of the biopsy resulting in prostate cancer diagnosis
Beschrijving

date of the biopsy

Datatype

date

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Similar models

Previous Clinical Trial Participation GSK study Prostatic neoplasms NCT00883909

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative data
Session number
Item
Session number
integer
Subject number
Item
Subject number
text
Item Group
Previous Clinical Trial Participation
Date of REDUCE 4 Year Contact
Item
Date of REDUCE 4 Year Contact
date
Date Investigational Product Stopped
Item
Date Investigational Product Stopped
date
Item
Was the subject previously diagnosed with prostate cancer during the REDUCE (ARI40006) study?
text
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 the biopsy
Item
If YES, record the date of the biopsy resulting in prostate cancer diagnosis
date
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