ID
26516
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)
- 18/10/2017 18/10/2017 -
Détendeur de droits
GSK
Téléchargé le
18 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
Screening Laboratory Collections
- StudyEvent: ODM
Description
Laboratory Collections for females only, ESTRADIOL and FSH - Ensure a blood sample has been taken for Estradiol and FSH.
Alias
- UMLS CUI-1
- C0014912
- UMLS CUI-3
- C0202022
Description
Date and Time of Blood sampling
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0040223
Description
Estradiol
Type de données
text
Alias
- UMLS CUI [1]
- C0014912
Description
FSH
Type de données
text
Alias
- UMLS CUI [1]
- C0202022
Description
Clinical Chemistry and Haematology
Alias
- UMLS CUI-1
- C0008000
- UMLS CUI-2
- C0474523
Description
Date | Time
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0005834
- UMLS CUI [2,1]
- C0040223
- UMLS CUI [2,2]
- C0005834
Description
Comment
Type de données
text
Alias
- UMLS CUI [1]
- C0947611
Description
Abnormal Value
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0205161
- UMLS CUI [1,2]
- C2826633
Description
Urinanalysis
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 values
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0205161
- UMLS CUI [1,2]
- C2826633
Description
Drug Screening (Urine)
Alias
- UMLS CUI-1
- C0202274
Description
Date | Time
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0200354
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0040223
Description
Drug Detection
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1444657
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C1511790
Description
Type of Drug
Type de données
text
Alias
- UMLS CUI [1]
- C0457591
Description
Comment
Type de données
text
Alias
- UMLS CUI [1]
- C0947611
Description
Ensure a 4ml blood sample has been taken to provide serum for screening for HIV antibodies, Hepatitis B surface antigen, Hepatitis C antibody.
Alias
- UMLS CUI-1
- C0019682
- UMLS CUI-2
- C0019163
- UMLS CUI-3
- C0019196
Description
URINE PREGNANCY TEST (Females only)
Alias
- UMLS CUI-1
- C0032976
Description
Pregnancy Test
Type de données
boolean
Alias
- UMLS CUI [1]
- C0032976
Description
Reason No
Type de données
text
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0032976
Description
Date | Time Pregnancy Test
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0430060
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0040223
Description
Result Pregnancy Test
Type de données
text
Alias
- UMLS CUI [1]
- C3259477
Similar models
Screening Laboratory Collections
- StudyEvent: ODM
C0202022 (UMLS CUI-3)
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C0005834 (UMLS CUI [1,2])
C0040223 (UMLS CUI [2,1])
C0005834 (UMLS CUI [2,2])
C2826633 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C2826633 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C1511790 (UMLS CUI [1,3])
C0019163 (UMLS CUI-2)
C0019196 (UMLS CUI-3)
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C0032976 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])