ID

38638

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. 29-10-19 29-10-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

29 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

Randomsation Number

  1. StudyEvent: ODM
    1. Randomsation Number
Randomisation
Beschrijving

Randomisation

Alias
UMLS CUI-1
C0034656
Was the subject able to be randomised?
Beschrijving

Randomization

Datatype

boolean

Alias
UMLS CUI [1]
C0034656
Yes, provide: Randomisation number
Beschrijving

Randomization, Numbers

Datatype

integer

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0237753
Yes, provide: Date of randomisation
Beschrijving

Randomization, Date in time

Datatype

date

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0011008

Similar models

Randomsation Number

  1. StudyEvent: ODM
    1. Randomsation Number
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Randomisation
C0034656 (UMLS CUI-1)
Randomization
Item
Was the subject able to be randomised?
boolean
C0034656 (UMLS CUI [1])
Randomization, Numbers
Item
Yes, provide: Randomisation number
integer
C0034656 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Randomization, Date in time
Item
Yes, provide: Date of randomisation
date
C0034656 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])

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