ID

27362

Descrizione

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

versioni (2)
  1. 09/11/17 09/11/17 -
  2. 26/11/17 26/11/17 -
Titolare del copyright

GlaxoSmithKline

Caricato su

9 novembre 2017

DOI

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Licenza

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

Inglese

Previous Clinical Trial Participation GSK study Prostatic neoplasms NCT00883909

1 moduli  
Administrative data
Descrizione

Administrative data

Session number
Descrizione

Session number

Tipo di dati

integer

Subject number
Descrizione

Subject number

Tipo di dati

text

Previous Clinical Trial Participation
Descrizione

Previous Clinical Trial Participation

Date of REDUCE 4 Year Contact
Descrizione

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 di dati

date

Date Investigational Product Stopped
Descrizione

Date Investigational Product Stopped

Tipo di dati

date

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

previous diagnosis of prostate cancer

Tipo di dati

text

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

date of the biopsy

Tipo di dati

date

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Similar models

Previous Clinical Trial Participation GSK study Prostatic neoplasms NCT00883909

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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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