ID
26661
Beschreibung
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
Stichworte
Versionen (1)
- 23.10.17 23.10.17 -
Rechteinhaber
GSK
Hochgeladen am
23. Oktober 2017
DOI
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Lizenz
Creative Commons BY-NC 3.0
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7% CO2, GW597599, paroxetine andor alprazolam in healthy volunteers 100690
Follow-Up
- StudyEvent: ODM
Beschreibung
URINE PREGNANCY TEST (Females only)
Alias
- UMLS CUI-1
- C0430056
Beschreibung
Urine Pregnancy Test
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0430056
Beschreibung
Reason
Datentyp
text
Alias
- UMLS CUI [1]
- C0430056
Beschreibung
Date Time
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0430057
- UMLS CUI [2,1]
- C0040223
- UMLS CUI [2,2]
- C0430057
Beschreibung
Result
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1274040
- UMLS CUI [1,2]
- C0430057
Beschreibung
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
Beschreibung
Date | Time
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0005834
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C0040223
Beschreibung
Comment
Datentyp
text
Alias
- UMLS CUI [1]
- C0947611
Beschreibung
Abnormal Findings
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C2826633
- UMLS CUI [2,1]
- C0474523
- UMLS CUI [2,2]
- C2826633
Beschreibung
Ensure a urine sample has been taken for urinalysis
Alias
- UMLS CUI-1
- C0042014
Beschreibung
Date | Time
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C0200354
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [2,1]
- C0200354
- UMLS CUI [2,2]
- C0040223
Beschreibung
Comment
Datentyp
text
Alias
- UMLS CUI [1]
- C0947611
Beschreibung
Abnormal findings
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C2826633
Ähnliche Modelle
Follow-Up
- StudyEvent: ODM
C0430057 (UMLS CUI [1,2])
C0040223 (UMLS CUI [2,1])
C0430057 (UMLS CUI [2,2])
C0430057 (UMLS CUI [1,2])
C0018941 (UMLS CUI-2)
C0005834 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
C2826633 (UMLS CUI [1,2])
C0474523 (UMLS CUI [2,1])
C2826633 (UMLS CUI [2,2])
C0011008 (UMLS CUI [1,2])
C0200354 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
C2826633 (UMLS CUI [1,2])