ID

27362

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

Keywords

Versions (2)
  1. 11/9/17 11/9/17 -
  2. 11/26/17 11/26/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

November 9, 2017

DOI

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License

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

English

Previous Clinical Trial Participation GSK study Prostatic neoplasms NCT00883909

1 forms  
Administrative data
Description

Administrative data

Session number
Description

Session number

Data type

integer

Subject number
Description

Subject number

Data type

text

Previous Clinical Trial Participation
Description

Previous Clinical Trial Participation

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

Data type

date

Date Investigational Product Stopped
Description

Date Investigational Product Stopped

Data type

date

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

previous diagnosis of prostate cancer

Data type

text

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

date of the biopsy

Data type

date

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Similar models

Previous Clinical Trial Participation GSK study Prostatic neoplasms NCT00883909

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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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