ID

31406

Beskrivning

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

Nyckelord

Versioner (1)
  1. 2018-08-19 2018-08-19 -
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see clinicaltrials.gov

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19 augusti 2018

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Creative Commons BY 4.0
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Emotional processing in healthy male volunteers treated with GSK424887 NCT01424384

Engelsk

Eligibility Question

1 Formulär  
  1. StudyEvent: ODM
    1. Eligibility Question
Eligibility Question
Beskrivning

Eligibility Question

Alias
UMLS CUI-1
C1516637
Did the subject meet all the entry criteria?
Beskrivning

Clinical Trial Eligibility Criteria

Datatyp

boolean

Alias
UMLS CUI [1]
C1516637
If subject did not meet all the entry criteria, please select all boxes corresponding to violations of any inclusion criteria
Beskrivning

Clinical Trial Eligibility Criteria; Inclusion; Protocol Violation

Datatyp

integer

Alias
UMLS CUI [1,1]
C1516637
UMLS CUI [1,2]
C1512693
UMLS CUI [1,3]
C1709750
If subject did not meet all the entry criteria, please select all boxes corresponding to violations of any exclusion criteria
Beskrivning

Clinical Trial Eligibility Criteria; Exclusion Criteria; Protocol Violation

Datatyp

integer

Alias
UMLS CUI [1,1]
C1516637
UMLS CUI [1,2]
C0680251
UMLS CUI [1,3]
C1709750
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Similar models

Eligibility Question

1 Formulär
  1. StudyEvent: ODM
    1. Eligibility Question
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Eligibility Question
C1516637 (UMLS CUI-1)
Clinical Trial Eligibility Criteria
Item
Did the subject meet all the entry criteria?
boolean
C1516637 (UMLS CUI [1])
Item
If subject did not meet all the entry criteria, please select all boxes corresponding to violations of any inclusion criteria
integer
C1516637 (UMLS CUI [1,1])
C1512693 (UMLS CUI [1,2])
C1709750 (UMLS CUI [1,3])
Clinical Trial Eligibility Criteria; Inclusion; Protocol Violation
Code List
If subject did not meet all the entry criteria, please select all boxes corresponding to violations of any inclusion criteria
CL Item
Inclusion Criteria 1 (1)
CL Item
Inclusion Criteria 2 (2)
CL Item
Inclusion Criteria 3 (3)
CL Item
Inclusion Criteria 4 (4)
CL Item
Inclusion Criteria 5 (5)
CL Item
Inclusion Criteria 6 (6)
CL Item
Inclusion Criteria 7 (7)
CL Item
Inclusion Criteria 8 (8)
CL Item
Inclusion Criteria 9 (9)
CL Item
Inclusion Criteria 10 (10)
Item
If subject did not meet all the entry criteria, please select all boxes corresponding to violations of any exclusion criteria
integer
C1516637 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
C1709750 (UMLS CUI [1,3])
Clinical Trial Eligibility Criteria; Exclusion Criteria; Protocol Violation
Code List
If subject did not meet all the entry criteria, please select all boxes corresponding to violations of any exclusion criteria
CL Item
Exclusion Criteria 1 (1)
CL Item
Exclusion Criteria 2 (2)
CL Item
Exclusion Criteria 3 (3)
CL Item
Exclusion Criteria 4 (4)
CL Item
Exclusion Criteria 5 (5)
CL Item
Exclusion Criteria 6 (6)
CL Item
Exclusion Criteria 7 (7)
CL Item
Exclusion Criteria 8 (8)
CL Item
Exclusion Criteria 9 (9)
CL Item
Exclusion Criteria 10 (10)
CL Item
Exclusion Criteria 11 (11)
CL Item
Exclusion Criteria 12 (12)
CL Item
Exclusion Criteria 13 (13)
CL Item
Exclusion Criteria 14 (14)
CL Item
Exclusion Criteria 15 (15)
CL Item
Exclusion Criteria 16 (16)
CL Item
Exclusion Criteria 17 (17)
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