ID
32027
Beskrivning
Study ID: 105548 Clinical Study ID: HZA105548 Study Title: A double-blind, randomized, placebo-controlled, repeat dose, 2-way crossover drug interaction study to investigate the pharmacokinetic and pharmacodynamic effects following administration of fluticasone furoate/GW642444M Inhalation Powder with ketoconazole Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01165125 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: fluticasone furoate/vilanterol; vilanterol Trade Name: Relvar; vilanterol Study Indication: Asthma
Nyckelord
Versioner (1)
- 2018-10-14 2018-10-14 -
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
14 oktober 2018
DOI
För en begäran logga in.
Licens
Creative Commons BY-NC 3.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
Pharmacokinetic and pharmacodynamic effects following administration of fluticasone Inhalation Powder with ketoconazole NCT01165125
Eligibility Question, Subject Identification, Electronically Transferred Lab Data Screening and Day 1 and Randomisation Number
Beskrivning
Inclusion Criteria
Alias
- UMLS CUI-1
- C1512693
Beskrivning
Inclusion
Datatyp
integer
Alias
- UMLS CUI [1]
- C1512693
Beskrivning
Exclusion Criteria
Alias
- UMLS CUI-1
- C0680251
Beskrivning
Exclusion Criteria
Datatyp
integer
Alias
- UMLS CUI [1]
- C0680251
Beskrivning
Subject Identification
Alias
- UMLS CUI-1
- C2348585
Beskrivning
Electronically transferred lab data - Screening
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C1320722
Beskrivning
Hematology Date and time sample taken
Datatyp
datetime
Alias
- UMLS CUI [1,1]
- C0018943
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Beskrivning
Clinical Chemistry Date and time sample taken
Datatyp
datetime
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Beskrivning
Urinalysis Date and time sample taken
Datatyp
datetime
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Beskrivning
Electronically transferred lab data - Day 1
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C1320722
Beskrivning
Hematology Date and time sample taken
Datatyp
datetime
Alias
- UMLS CUI [1,1]
- C0018943
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Beskrivning
Clinical Chemistry Date and time sample taken
Datatyp
datetime
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Beskrivning
Randomisation number
Alias
- UMLS CUI-1
- C1300638
- UMLS CUI-2
- C0034656
Beskrivning
Randomisation; Ability
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0034656
- UMLS CUI [1,2]
- C0085732
Beskrivning
Randomisation Number
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0034656
- UMLS CUI [1,2]
- C0085732
- UMLS CUI [2,1]
- C1300638
- UMLS CUI [2,2]
- C0034656
Beskrivning
Date of randomisation
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0034656
- UMLS CUI [1,2]
- C0011008
Similar models
Eligibility Question, Subject Identification, Electronically Transferred Lab Data Screening and Day 1 and Randomisation Number
C1709750 (UMLS CUI [2,1])
C0680251 (UMLS CUI [2,2])
C1709750 (UMLS CUI [3,1])
C1512693 (UMLS CUI [3,2])
C1516637 (UMLS CUI [3,3])
C1320722 (UMLS CUI-2)
C0200345 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0200345 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0200345 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C1320722 (UMLS CUI-2)
C0200345 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0200345 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0085732 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,2])
C1300638 (UMLS CUI [2,1])
C0034656 (UMLS CUI [2,2])
C0011008 (UMLS CUI [1,2])