ID

38136

Description

Study ID: 105036 Clinical Study ID: 105036 Study Title: A single-blind, randomized, placebo-controlled study to investigate the safety, tolerability, and potential effects on betamethasone pharmacokinetics of a co-administered infusion of GSK221149A in healthy female subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: betamethasone Trade Name: Retosiban Study Indication: Women's Health & Pregnancy - Other, pre-term labour

Keywords

Versions (1)
  1. 9/21/19 9/21/19 -
Copyright Holder

GlaxoSmithKline

Uploaded on

September 21, 2019

DOI

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License

Creative Commons BY-NC 3.0
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Betamethasone pharmacokinetics of a co-administered infusion of GSK221149A; 105036

English

Electronically Transferred Lab Data (Lab 24hr)

1 forms  
Dosing Date and Time
Description

Dosing Date and Time

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0178602
UMLS CUI-3
C0011008
UMLS CUI-4
C0040223
Dosing date/time
Description

Laboratory Procedures, Dosage, Date in time, Time

Data type

datetime

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0011008
UMLS CUI [1,4]
C0040223
24 Hours Post Dose
Description

24 Hours Post Dose

Alias
UMLS CUI-1
C0022885
UMLS CUI-2
C0439568
UMLS CUI-3
C1442770
Hematology Date and Time sample taken
Description

Hematology, Post-dose, 24 Hours, Sampling, Date in time, Time

Data type

datetime

Alias
UMLS CUI [1,1]
C0474523
UMLS CUI [1,2]
C0439568
UMLS CUI [1,3]
C1442770
UMLS CUI [1,4]
C0870078
UMLS CUI [1,5]
C0011008
UMLS CUI [1,6]
C0040223
Clinical Chemistry Date and Time sample taken
Description

Chemistry, Clinical, Post-dose, 24 Hours, Sampling, Date in time, Time

Data type

datetime

Alias
UMLS CUI [1,1]
C0008000
UMLS CUI [1,2]
C0439568
UMLS CUI [1,3]
C1442770
UMLS CUI [1,4]
C0870078
UMLS CUI [1,5]
C0011008
UMLS CUI [1,6]
C0040223
Urinalysis Date and Time sample taken
Description

Urinalysis, Post-dose, 24 Hours, Sampling, Date in time, Time

Data type

datetime

Alias
UMLS CUI [1,1]
C0042014
UMLS CUI [1,2]
C0439568
UMLS CUI [1,3]
C1442770
UMLS CUI [1,4]
C0870078
UMLS CUI [1,5]
C0011008
UMLS CUI [1,6]
C0040223
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Similar models

Electronically Transferred Lab Data (Lab 24hr)

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Dosing Date and Time
C0022885 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
C0011008 (UMLS CUI-3)
C0040223 (UMLS CUI-4)
Laboratory Procedures, Dosage, Date in time, Time
Item
Dosing date/time
datetime
C0022885 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Item Group
24 Hours Post Dose
C0022885 (UMLS CUI-1)
C0439568 (UMLS CUI-2)
C1442770 (UMLS CUI-3)
Hematology, Post-dose, 24 Hours, Sampling, Date in time, Time
Item
Hematology Date and Time sample taken
datetime
C0474523 (UMLS CUI [1,1])
C0439568 (UMLS CUI [1,2])
C1442770 (UMLS CUI [1,3])
C0870078 (UMLS CUI [1,4])
C0011008 (UMLS CUI [1,5])
C0040223 (UMLS CUI [1,6])
Chemistry, Clinical, Post-dose, 24 Hours, Sampling, Date in time, Time
Item
Clinical Chemistry Date and Time sample taken
datetime
C0008000 (UMLS CUI [1,1])
C0439568 (UMLS CUI [1,2])
C1442770 (UMLS CUI [1,3])
C0870078 (UMLS CUI [1,4])
C0011008 (UMLS CUI [1,5])
C0040223 (UMLS CUI [1,6])
Urinalysis, Post-dose, 24 Hours, Sampling, Date in time, Time
Item
Urinalysis Date and Time sample taken
datetime
C0042014 (UMLS CUI [1,1])
C0439568 (UMLS CUI [1,2])
C1442770 (UMLS CUI [1,3])
C0870078 (UMLS CUI [1,4])
C0011008 (UMLS CUI [1,5])
C0040223 (UMLS CUI [1,6])
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