ID
26519
Description
Study ID: 100690 Clinical Study ID: NKP100690 Study Title: A randomised, double blind triple dummy, placebo controlled balanced incomplete block crossover study to evaluate the change in response to a 7% CO2 challenge and pharmacokinetics of single oral doses of GW597599 and paroxetine (5 or 7.5 mg) either alone or in combination, or alprazolam (0.75 mg) in healthy volunteers Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 1 Study Recruitment Status: Completed Generic Name: paroxetine Trade Name: Tagonis,Seroxat,Paxil,Paroxat,Deroxat,Aropax Study Indication: Depressive Disorder and Anxiety Disorders CRF Seiten: 255-365
Keywords
Versions (1)
- 10/18/17 10/18/17 -
Copyright Holder
GSK
Uploaded on
October 18, 2017
DOI
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License
Creative Commons BY-NC 3.0
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7% CO2, GW597599, paroxetine andor alprazolam in healthy volunteers 100690
Screening; Significant medical/surgical history and physical examination
Description
Significant medical/surgical history and physical examination
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C0031809
Description
Medical History
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0750502
Description
Significant medical/surgical history and physical examination
Alias
- UMLS CUI-1
- C0262926
- UMLS CUI-2
- C0031809
Description
Diagnosis
Data type
text
Alias
- UMLS CUI [1]
- C0011900
Description
GSK Use
Data type
text
Description
Year of first diagnosis
Data type
partialDate
Alias
- UMLS CUI [1,1]
- C0439234
- UMLS CUI [1,2]
- C0011900
Description
Past disease
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1444637
- UMLS CUI [1,2]
- C0012634
Description
Ongoing Disease
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0549178
- UMLS CUI [1,2]
- C0012634
Description
GSK Use
Data type
text
Description
Semi-Supine Vital Signs
Alias
- UMLS CUI-1
- C0518766
Description
Study Time
Data type
text
Alias
- UMLS CUI [1,1]
- C2348563
- UMLS CUI [1,2]
- C0040223
Description
Date
Data type
date
Alias
- UMLS CUI [1]
- C0011008
Description
Time
Data type
time
Measurement units
- 24hr:min
Alias
- UMLS CUI [1]
- C0040223
Description
Systolic Blood Pressure
Data type
text
Measurement units
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Description
Diastolic Blood Pressure
Data type
text
Measurement units
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Description
12-Lead ECG Monitoring
Alias
- UMLS CUI-1
- C0430456
Description
Study Time
Data type
text
Alias
- UMLS CUI [1,1]
- C2348563
- UMLS CUI [1,2]
- C0040223
Description
Date
Data type
date
Alias
- UMLS CUI [1]
- C0011008
Description
Time
Data type
time
Measurement units
- 24hr:min
Alias
- UMLS CUI [1]
- C0040223
Description
Heart Rate
Data type
text
Measurement units
- bpm
Alias
- UMLS CUI [1]
- C0018810
Description
PR
Data type
text
Measurement units
- msec
Alias
- UMLS CUI [1]
- C0429087
Description
QRS
Data type
text
Measurement units
- msec
Alias
- UMLS CUI [1]
- C1880451
Description
QT
Data type
text
Measurement units
- msec
Alias
- UMLS CUI [1]
- C1287082
Description
QTc
Data type
text
Measurement units
- msec
Alias
- UMLS CUI [1]
- C0489625
Description
ECG normal
Data type
boolean
Alias
- UMLS CUI [1]
- C0522054
Description
Comments
Data type
text
Alias
- UMLS CUI [1]
- C0947611
Description
12-Lead Continous Electrocardiographic Monitoring
Alias
- UMLS CUI-1
- C0430456
- UMLS CUI-2
- C4055630
Description
Start Date
Data type
date
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C4055630
Description
Start time
Data type
time
Measurement units
- 24hr:min
Alias
- UMLS CUI [1,1]
- C1301880
- UMLS CUI [1,2]
- C4055630
Description
Stop Date
Data type
date
Alias
- UMLS CUI [1,1]
- C0806020
- UMLS CUI [1,2]
- C4055630
Description
Stop Time
Data type
time
Measurement units
- 24hr:min
Alias
- UMLS CUI [1,1]
- C1522314
- UMLS CUI [1,2]
- C4055630
Description
Rhythms of Concern
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0420200
- UMLS CUI [1,2]
- C0871269
- UMLS CUI [1,3]
- C2699424
Description
Rhythm of Concern Description
Data type
text
Alias
- UMLS CUI [1,1]
- C0420200
- UMLS CUI [1,2]
- C0871269
- UMLS CUI [1,3]
- C2699424
- UMLS CUI [1,4]
- C0678257
Similar models
Screening; Significant medical/surgical history and physical examination
C0031809 (UMLS CUI-2)
C0750502 (UMLS CUI [1,2])
C0031809 (UMLS CUI-2)
C0011900 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,2])
C4055630 (UMLS CUI-2)
C4055630 (UMLS CUI [1,2])
C4055630 (UMLS CUI [1,2])
C4055630 (UMLS CUI [1,2])
C4055630 (UMLS CUI [1,2])
C0871269 (UMLS CUI [1,2])
C2699424 (UMLS CUI [1,3])
C0871269 (UMLS CUI [1,2])
C2699424 (UMLS CUI [1,3])
C0678257 (UMLS CUI [1,4])