ID
26652
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
Mots-clés
Versions (1)
- 23/10/2017 23/10/2017 -
Détendeur de droits
GSK
Téléchargé le
23 octobre 2017
DOI
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Licence
Creative Commons BY-NC 3.0
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7% CO2, GW597599, paroxetine andor alprazolam in healthy volunteers 100690
Session 3 Day 1 Pre-Dose
- StudyEvent: ODM
Description
Urine Pregnancy Test (Females only)
Alias
- UMLS CUI-1
- C0430056
Description
Urine Pregnancy Test
Type de données
boolean
Alias
- UMLS CUI [1]
- C0430056
Description
undefined item
Type de données
text
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0032976
Description
Date | Time
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0040223
- UMLS CUI [1,3]
- C0032976
Description
Test result
Type de données
text
Alias
- UMLS CUI [1,1]
- C0456984
- UMLS CUI [1,2]
- C0032976
Description
Clinical Chemistry and Haematology ensure a blood sample has been taken tor clinical chemistry and haematology
Alias
- UMLS CUI-1
- C0008000
- UMLS CUI-2
- C0018941
Description
Date | Time
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0040223
Description
Comment
Type de données
text
Alias
- UMLS CUI [1]
- C0947611
Description
Abnormal Lab values
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0438215
- UMLS CUI [1,2]
- C2826293
Description
Urinalysis Ensure a urine sample has been taken tor clinical chemistry and haematology
Alias
- UMLS CUI-1
- C0042014
Description
Date | Time
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0200354
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0040223
Description
Comment
Type de données
text
Alias
- UMLS CUI [1]
- C0947611
Description
Abnormal test results
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0438215
- UMLS CUI [1,2]
- C2826293
Similar models
Session 3 Day 1 Pre-Dose
- StudyEvent: ODM
C0032976 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C0032976 (UMLS CUI [1,3])
C0032976 (UMLS CUI [1,2])
C0018941 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C2826293 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C2826293 (UMLS CUI [1,2])