ID
38530
Description
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
Keywords
Versions (2)
- 10/24/19 10/24/19 -
- 10/24/19 10/24/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
October 24, 2019
DOI
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License
Creative Commons BY-NC 3.0
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Efficacy and Safety of GSK163090 in Subjects with Major Depressive Disorder; NCT00896363
End of Study
- StudyEvent: ODM
Description
Date of Visit/Assessment
Alias
- UMLS CUI-1
- C1320303
- UMLS CUI-2
- C2985720
Description
Pharmacogenetic (PGx) Research Withdrawal of Consent
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-2
- C0021430
- UMLS CUI-3
- C2349954
Description
Pharmacogenetic Test, Informed Consent, Withdraw
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C2349954
Description
Pharmacogenetic Test, Informed Consent, Withdraw, Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C2349954
- UMLS CUI [1,4]
- C0011008
Description
Pharmacogenetic Test, Blood specimen, Destruction, Request
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
Description
Pharmacogenetic Test, Blood specimen, Destruction, Request, Reason and justification
Data type
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
- UMLS CUI [1,5]
- C0566251
Description
Pharmacogenetic Test, Blood specimen, Destruction, Request, Reason and justification
Data type
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
- UMLS CUI [1,5]
- C0566251
Description
Status of Treatment Blind
Alias
- UMLS CUI-1
- C2347038
- UMLS CUI-2
- C0449438
Description
Blinded Clinical Study, Subject Unblinding Event Record
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
Description
Blinded Clinical Study, Subject Unblinding Event Record, Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
- UMLS CUI [1,3]
- C0011008
Description
Blinded Clinical Study, Subject Unblinding Event Record, Reason and justification
Data type
text
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
- UMLS CUI [1,3]
- C0566251
Description
Blinded Clinical Study, Subject Unblinding Event Record, Reason and justification
Data type
text
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
- UMLS CUI [1,3]
- C0566251
Description
Medical Device Question
Alias
- UMLS CUI-1
- C0025080
- UMLS CUI-2
- C1522634
Description
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Description
Study Conclusion
Alias
- UMLS CUI-1
- C0008976
- UMLS CUI-2
- C1707478
Description
Completion Status, Date in time; Withdraw, Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C0805732
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [2,1]
- C2349954
- UMLS CUI [2,2]
- C0011008
Description
Patient withdrawn from trial
Data type
boolean
Alias
- UMLS CUI [1]
- C0422727
Description
Patient withdrawn from trial, Reason and justification, Primary
Data type
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [1,3]
- C0205225
Description
Patient withdrawn from trial, Reason and justification, Primary
Data type
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [1,3]
- C0205225
Description
Clinical study case, Investigator Signature
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1706256
- UMLS CUI [1,2]
- C2346576
Similar models
End of Study
- StudyEvent: ODM
C1300638 (UMLS CUI [1,2])
C2985720 (UMLS CUI-2)
C2985720 (UMLS CUI [2])
C0021430 (UMLS CUI-2)
C2349954 (UMLS CUI-3)
C0021430 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0566251 (UMLS CUI [1,5])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0566251 (UMLS CUI [1,5])
C0449438 (UMLS CUI-2)
C3897431 (UMLS CUI [1,2])
C3897431 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C3897431 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C3897431 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C1522634 (UMLS CUI-2)
C1551358 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C2349954 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C0566251 (UMLS CUI [1,2])
C0205225 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,2])
C0205225 (UMLS CUI [1,3])
C2346576 (UMLS CUI [1,2])