ID
24050
Beschreibung
Study ID: 100716 Clinical Study ID: NKP100716 Study Title: An open label repeat dose study to investigate the effect of GW597599 (15 mg) and paroxetine (10 mg) given in combination for 15 days on the pharmacokinetics of midazolam and dextromethorphan in healthy male and female 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: vestipitant Trade Name: paroxetine and vestipitant Study Indication: Depressive Disorder and Anxiety Disorders Documentation part: Pharmacogenetic Research, Prior And Concomitant Medication, Baseline Signs and Symptoms
Stichworte
Versionen (2)
- 24.07.17 24.07.17 -
- 20.09.21 20.09.21 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
24. Juli 2017
DOI
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Lizenz
Creative Commons BY-NC 3.0
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GW597599 and paroxetine on the pharmacokinetics of midazolam and dextromethorphan 100716 Pharmacogenetic Research, Prior And Concomitant Medication, Baseline Signs And Symptoms
GW597599 and paroxetine on the pharmacokinetics of midazolam and dextromethorphan 100716 Pharmacogenetic Research, Prior And Concomitant Medication, Baseline Signs And Symptoms
Beschreibung
Prior Medication
Alias
- UMLS CUI-1
- C0013227
Beschreibung
If Yes, please record the medications below.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0013227
Beschreibung
drug name
Datentyp
text
Alias
- UMLS CUI [1]
- C0013227
Beschreibung
dosage
Datentyp
text
Alias
- UMLS CUI [1]
- C0178602
Beschreibung
frequency of this dose
Datentyp
text
Alias
- UMLS CUI [1]
- C3476109
Beschreibung
administration route
Datentyp
text
Alias
- UMLS CUI [1]
- C0013153
Beschreibung
medication indication
Datentyp
text
Alias
- UMLS CUI [1]
- C3146298
Beschreibung
duration of therapy
Datentyp
text
Alias
- UMLS CUI [1]
- C0444917
Beschreibung
medication end date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0806020
- UMLS CUI [1,2]
- C0013227
Beschreibung
continuing medication at end of study
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1553904
Beschreibung
Baseline Signs Ans Symptoms
Alias
- UMLS CUI-1
- C0037088
- UMLS CUI-2
- C1442488
Beschreibung
diagnosis
Datentyp
text
Alias
- UMLS CUI [1]
- C0011900
Beschreibung
onset date and time
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C2981441
- UMLS CUI [1,2]
- C1442488
Beschreibung
end date and time
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C2981425
- UMLS CUI [1,2]
- C1442488
Beschreibung
outcome
Datentyp
text
Alias
- UMLS CUI [1]
- C1705586
Beschreibung
event course
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0750729
Beschreibung
intensity
Datentyp
text
Alias
- UMLS CUI [1]
- C0518690
Beschreibung
relationship to study procedures
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C1510821
Beschreibung
If Yes, please record on Prior Medication form.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0559546
- UMLS CUI [1,2]
- C0087111
Beschreibung
subject withdrawn due to event
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0877248
Ähnliche Modelle
GW597599 and paroxetine on the pharmacokinetics of midazolam and dextromethorphan 100716 Pharmacogenetic Research, Prior And Concomitant Medication, Baseline Signs And Symptoms
C0021430 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0178913 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C1442488 (UMLS CUI-2)
C1442488 (UMLS CUI [1,2])
C1442488 (UMLS CUI [1,2])
C1510821 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,2])