ID

38741

Beschrijving

Study ID: 109035 Clinical Study ID: 109035 Study Title: A Randomised, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy and Safety of GSK163090 in Subjects With Major Depressive Disorder Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00896363 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: GSK163090 1 mg, GSK163090 Placebo, GSK163090 3 mg Trade Name: Study Indication: Depressive Disorder

Trefwoorden

  1. 31-10-19 31-10-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

31 oktober 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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Efficacy and Safety of GSK163090 in Subjects with Major Depressive Disorder; NCT00896363

Status of Treatment Blind

Status of Treatment Blind
Beschrijving

Status of Treatment Blind

Alias
UMLS CUI-1
C2347038
UMLS CUI-2
C0449438
Was the treatment blind broken during the study?
Beschrijving

Subject Unblinding Event Record

Datatype

boolean

Alias
UMLS CUI [1]
C3897431
Yes, Date/time blind broken
Beschrijving

Subject Unblinding Event Record, Date in time, Time

Datatype

datetime

Alias
UMLS CUI [1,1]
C3897431
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C0040223
Yes, Reason blind broken
Beschrijving

Subject Unblinding Event Record, Reason and justification

Datatype

text

Alias
UMLS CUI [1,1]
C3897431
UMLS CUI [1,2]
C0566251
Other, specify
Beschrijving

Subject Unblinding Event Record, Reason and justification

Datatype

text

Alias
UMLS CUI [1,1]
C3897431
UMLS CUI [1,2]
C0566251

Similar models

Status of Treatment Blind

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Status of Treatment Blind
C2347038 (UMLS CUI-1)
C0449438 (UMLS CUI-2)
Subject Unblinding Event Record
Item
Was the treatment blind broken during the study?
boolean
C3897431 (UMLS CUI [1])
Subject Unblinding Event Record, Date in time, Time
Item
Yes, Date/time blind broken
datetime
C3897431 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Item
Yes, Reason blind broken
text
C3897431 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])
CL Item
Medical emergency requiring identification of investigational product for further investigation (1)
CL Item
Other, specify (2)
Subject Unblinding Event Record, Reason and justification
Item
Other, specify
text
C3897431 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])

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