ID

27475

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

  1. 11/15/17 11/15/17 -
  2. 11/26/17 11/26/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

November 15, 2017

DOI

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License

Creative Commons BY-NC 3.0

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Investigator data Log GSK study Prostatic neoplasms NCT00883909

Investigator data Log GSK study Prostatic neoplasms NCT00883909

Administrative data
Description

Administrative data

Session number
Description

Session number

Data type

integer

Subject number
Description

Subject number

Data type

text

Investigator Comment Log
Description

Investigator Comment Log

Date of comment
Description

Date of comment

Data type

date

CRF page number if applicable
Description

CRF page number

Data type

integer

Comment
Description

Comment

Data type

text

Investigator’s Statement
Description

Investigator’s Statement

Date
Description

Check that the date of signature is on or after the completion of Visit 10.

Data type

date

Investigator’s Signature
Description

Sign and date this page after all relevant CRF pages, including outstanding test results, are completed.

Data type

text

Investigator’s Name - Print
Description

Investigator Name

Data type

text

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Investigator data Log GSK study Prostatic neoplasms NCT00883909

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
Investigator Comment Log
Date of comment
Item
Date of comment
date
CRF page number
Item
CRF page number if applicable
integer
Comment
Item
Comment
text
Item Group
Investigator’s Statement
Date
Item
Date
date
Investigator Signature
Item
Investigator’s Signature
text
Investigator Name
Item
Investigator’s Name - Print
text

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