ID

31428

Description

Study ID: 105012 Clinical Study ID: NSS105012 Study Title: Emotional processing in healthy male volunteers treated with GSK424887. A single centre, randomised, double-blind, placebo-controlled parallel group study Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01424384 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: GSK424887 Trade Name: Citalopram Study Indication: Depressive Disorder and Anxiety Disorders

Keywords

Versions (1)
  1. 8/21/18 8/21/18 -
Copyright Holder

GlaxoSmithKline

Uploaded on

August 21, 2018

DOI

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License

Creative Commons BY-NC 3.0
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Emotional processing in healthy male volunteers treated with GSK424887 NCT01424384

English

Status of Treatment blind

1 forms  
Status of Treatment blind
Description

Status of Treatment blind

Alias
UMLS CUI-1
C0749659
UMLS CUI-2
C2347038
Was the treatment blind broken during the study? If yes, complete the Adverse Event form and/ or Investigational Product forms as appropriate.
Description

Subject Unblinding Event Record

Data type

boolean

Alias
UMLS CUI [1]
C3897431
If treatment blind was broken, date and time blind broken
Description

Subject Unblinding Event Record; Date in time | Subject Unblinding Event Record; Time

Data type

datetime

Alias
UMLS CUI [1,1]
C3897431
UMLS CUI [1,2]
C0011008
UMLS CUI [2,1]
C3897431
UMLS CUI [2,2]
C0040223
If treatment blind was broken, reason blind broken
Description

Subject Unblinding Event Record; Indication of (contextual qualifier)

Data type

integer

Alias
UMLS CUI [1,1]
C3897431
UMLS CUI [1,2]
C0392360
If other reason for treatment blind broken, please specify.
Description

Subject Unblinding Event Record; Indication of (contextual qualifier); Other; Specification

Data type

text

Alias
UMLS CUI [1,1]
C3897431
UMLS CUI [1,2]
C0392360
UMLS CUI [1,3]
C0205394
UMLS CUI [1,4]
C2348235
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Similar models

Status of Treatment blind

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Status of Treatment blind
C0749659 (UMLS CUI-1)
C2347038 (UMLS CUI-2)
Subject Unblinding Event Record
Item
Was the treatment blind broken during the study? If yes, complete the Adverse Event form and/ or Investigational Product forms as appropriate.
boolean
C3897431 (UMLS CUI [1])
Subject Unblinding Event Record; Date in time | Subject Unblinding Event Record; Time
Item
If treatment blind was broken, date and time blind broken
datetime
C3897431 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C3897431 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
Item
If treatment blind was broken, reason blind broken
integer
C3897431 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Subject Unblinding Event Record; Indication of (contextual qualifier)
Code List
If treatment blind was broken, reason blind broken
CL Item
Medical emergency requiring identification of investigational product for further treatment (1)
CL Item
Other (2)
Subject Unblinding Event Record; Indication of (contextual qualifier); Other; Specification
Item
If other reason for treatment blind broken, please specify.
text
C3897431 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
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