ID

27362

Descrição

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

Palavras-chave

Versões (2)
  1. 09/11/2017 09/11/2017 -
  2. 26/11/2017 26/11/2017 -
Titular dos direitos

GlaxoSmithKline

Transferido a

9 de novembro de 2017

DOI

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Licença

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

Inglês

Previous Clinical Trial Participation GSK study Prostatic neoplasms NCT00883909

1 Formulários  
Administrative data
Descrição

Administrative data

Session number
Descrição

Session number

Tipo de dados

integer

Subject number
Descrição

Subject number

Tipo de dados

text

Previous Clinical Trial Participation
Descrição

Previous Clinical Trial Participation

Date of REDUCE 4 Year Contact
Descrição

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 dados

date

Date Investigational Product Stopped
Descrição

Date Investigational Product Stopped

Tipo de dados

date

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

previous diagnosis of prostate cancer

Tipo de dados

text

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

date of the biopsy

Tipo de dados

date

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Similar models

Previous Clinical Trial Participation GSK study Prostatic neoplasms NCT00883909

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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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