ID

27670

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

26 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

Alias
UMLS CUI-1
C1320722
Session number
Beschrijving

Session number

Datatype

integer

Alias
UMLS CUI [1,1]
C1883017
UMLS CUI [1,2]
C0750480
Subject number
Beschrijving

Subject number

Datatype

text

Alias
UMLS CUI [1]
C2348585
Previous Clinical Trial Participation
Beschrijving

Previous Clinical Trial Participation

Alias
UMLS CUI-1
C2348568
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

Alias
UMLS CUI [1]
C1320303
Date Investigational Product Stopped
Beschrijving

Date Investigational Product Stopped

Datatype

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0304229
UMLS CUI [1,3]
C0457454
Was the subject previously diagnosed with prostate cancer during the REDUCE (ARI40006) study?
Beschrijving

previous diagnosis of prostate cancer

Datatype

text

Alias
UMLS CUI [1,1]
C0332132
UMLS CUI [1,2]
C0600139
If YES, record the date of the biopsy resulting in prostate cancer diagnosis
Beschrijving

date of biopsy

Datatype

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0005558
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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
C1320722 (UMLS CUI-1)
Session number
Item
Session number
integer
C1883017 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
Subject number
Item
Subject number
text
C2348585 (UMLS CUI [1])
Item Group
Previous Clinical Trial Participation
C2348568 (UMLS CUI-1)
Date of visit
Item
Date of REDUCE 4 Year Contact
date
C1320303 (UMLS CUI [1])
Date Investigational Product Stopped
Item
Date Investigational Product Stopped
date
C0011008 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
C0457454 (UMLS CUI [1,3])
Item
Was the subject previously diagnosed with prostate cancer during the REDUCE (ARI40006) study?
text
C0332132 (UMLS CUI [1,1])
C0600139 (UMLS CUI [1,2])
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 biopsy
Item
If YES, record the date of the biopsy resulting in prostate cancer diagnosis
date
C0011008 (UMLS CUI [1,1])
C0005558 (UMLS CUI [1,2])
Terug naar het begin van de pagina 

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