ID
39348
Description
Study ID: 110792 Clinical Study ID: 110792 Study Title: A placebo-controlled, single-blind, randomised study to investigate the safety, tolerability, pharmacokinetics and drug interaction of GSK1034702 after repeat doses in healthy subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00950586 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Dextromethorphan, Placebo Trade Name: N/A Study Indication: Cognitive Disorders
Keywords
Versions (1)
- 12/27/19 12/27/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
December 27, 2019
DOI
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License
Creative Commons BY-NC 3.0
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GSK1034702 after Repeat Doses in Healthy Subjects; NCT00950586
Follow-up
- StudyEvent: ODM
Description
Vital Signs Semi-supine
Alias
- UMLS CUI-1
- C0518766
- UMLS CUI-2
- C0522019
Description
Vital signs, Semi-erect, Date in time, Time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0522019
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Description
Systolic Pressure, Semi-erect
Data type
integer
Measurement units
- mm[Hg]
Alias
- UMLS CUI [1,1]
- C0871470
- UMLS CUI [1,2]
- C0522019
Description
Diastolic blood pressure, Semi-erect
Data type
integer
Measurement units
- mm[Hg]
Alias
- UMLS CUI [1,1]
- C0428883
- UMLS CUI [1,2]
- C0522019
Description
Heart rate, Semi-erect
Data type
integer
Measurement units
- bpm
Alias
- UMLS CUI [1,1]
- C0018810
- UMLS CUI [1,2]
- C0522019
Description
Respiratory rate, Semi-erect
Data type
integer
Measurement units
- breaths/min
Alias
- UMLS CUI [1,1]
- C0231832
- UMLS CUI [1,2]
- C0522019
Description
Vital Signs Standing
Alias
- UMLS CUI-1
- C0518766
- UMLS CUI-2
- C0522014
Description
Vital signs, Erect, Date in time, Time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0522014
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Description
Systolic Pressure, Erect
Data type
integer
Measurement units
- mm[Hg]
Alias
- UMLS CUI [1,1]
- C0871470
- UMLS CUI [1,2]
- C0522014
Description
Diastolic blood pressure, Erect
Data type
integer
Measurement units
- mm[Hg]
Alias
- UMLS CUI [1,1]
- C0428883
- UMLS CUI [1,2]
- C0522014
Description
Heart rate, Erect
Data type
integer
Measurement units
- bpm
Alias
- UMLS CUI [1,1]
- C0018810
- UMLS CUI [1,2]
- C0522014
Description
Pulmonary Function Tests
Alias
- UMLS CUI-1
- C0024119
Description
Pulmonary function tests, Date in time, Time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0024119
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0040223
Description
Pulmonary function tests; Forced expiratory volume in 1 second finding
Data type
text
Alias
- UMLS CUI [1,1]
- C0024119
- UMLS CUI [1,2]
- C0429706
Description
Pulmonary function tests, Vital capacity, Forced Vital Capacity
Data type
text
Alias
- UMLS CUI [1,1]
- C0024119
- UMLS CUI [1,2]
- C0042834
- UMLS CUI [1,3]
- C3714541
Description
Pulmonary function tests, Forced expired volume in one second/vital capacity ratio
Data type
text
Alias
- UMLS CUI [1,1]
- C0024119
- UMLS CUI [1,2]
- C0429744
Description
Status of Treatment Blind
Alias
- UMLS CUI-1
- C2347038
- UMLS CUI-2
- C0449438
Description
Subject Unblinding Event Record
Data type
boolean
Alias
- UMLS CUI [1]
- C3897431
Description
Subject Unblinding Event Record, Date in time, Time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0040223
Description
Subject Unblinding Event Record, Reason and justification
Data type
text
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0040223
Description
Subject Unblinding Event Record, Reason and justification
Data type
text
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0040223
Description
Study Conclusion
Alias
- UMLS CUI-1
- C0008972
- UMLS CUI-2
- C1707478
Description
Date last contact
Data type
date
Alias
- UMLS CUI [1]
- C0805839
Description
Patient withdrawn from trial
Data type
boolean
Alias
- UMLS CUI [1]
- C0422727
Description
Patient withdrawn from trial, Decision, Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0679006
- UMLS CUI [1,3]
- C0011008
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, Signature
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1706256
- UMLS CUI [1,2]
- C1519316
Description
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Description
Pregnancy, During, Clinical Trials
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0032961
- UMLS CUI [1,2]
- C0347984
- UMLS CUI [1,3]
- C0008976
Description
Pregnancy of partner, During, Clinical Trials
Data type
text
Alias
- UMLS CUI [1,1]
- C0919624
- UMLS CUI [1,2]
- C0347984
- UMLS CUI [1,3]
- C0008976
Description
Electronically Transferred Lab Data
Alias
- UMLS CUI-1
- C0022885
Description
Hematology finding, Sampling, Date in time, Time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0474523
- UMLS CUI [1,2]
- C0870078
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Description
Hematology finding, Sampling, Not Done
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0474523
- UMLS CUI [1,2]
- C0870078
- UMLS CUI [1,3]
- C1272696
Description
Chemistry, Clinical, Sampling, Date in time, Time
Data type
text
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0870078
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Description
Chemistry, Clinical, Sampling, Date in time, Time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0870078
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Description
Chemistry, Clinical, Sampling, Not Done
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0870078
- UMLS CUI [1,3]
- C1272696
Description
Urinalysis, Sampling, Date in time, Time
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0870078
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Description
Urinalysis, Sampling, Not Done
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0870078
- UMLS CUI [1,3]
- C1272696
Similar models
Follow-up
- StudyEvent: ODM
C2985720 (UMLS CUI [1,2])
C0522019 (UMLS CUI-2)
C0522019 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0522019 (UMLS CUI [1,2])
C0522019 (UMLS CUI [1,2])
C0522019 (UMLS CUI [1,2])
C0522019 (UMLS CUI [1,2])
C0522014 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0522014 (UMLS CUI [1,2])
C0522014 (UMLS CUI [1,2])
C0522014 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C0429706 (UMLS CUI [1,2])
C0042834 (UMLS CUI [1,2])
C3714541 (UMLS CUI [1,3])
C0429744 (UMLS CUI [1,2])
C0449438 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C1707478 (UMLS CUI-2)
C0679006 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,2])
C0205225 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,2])
C0205225 (UMLS CUI [1,3])
C1519316 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0347984 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0870078 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,3])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0870078 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,3])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0870078 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,3])