ID

38137

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

Investigational Product - IV Dosing

1 forms  
GSK221149A IV Dose - Rapid Infusion
Description

GSK221149A IV Dose - Rapid Infusion

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C0178602
UMLS CUI-3
C0456962
Start Date and Time
Description

Experimental drug, Dosage, Rapid, Start Date, Start time

Data type

datetime

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0456962
UMLS CUI [1,4]
C0808070
UMLS CUI [1,5]
C1301880
Stop Date and Time
Description

Experimental drug, Dosage, Rapid, End Date, End time

Data type

datetime

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0456962
UMLS CUI [1,4]
C0806020
UMLS CUI [1,5]
C1522314
GSK221149A IV Dose - Continuous (post rapid) infusion
Description

GSK221149A IV Dose - Continuous (post rapid) infusion

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C0178602
UMLS CUI-3
C0549178
Start Date and Time
Description

Experimental drug, Dosage, Continuous, Start Date, Start time

Data type

datetime

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0549178
UMLS CUI [1,4]
C0808070
UMLS CUI [1,5]
C1301880
Stop Date and Time
Description

Experimental drug, Dosage, Continuous, End Date, End time

Data type

datetime

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0549178
UMLS CUI [1,4]
C0806020
UMLS CUI [1,5]
C1522314
Betamethasone 10.6 mg IV Dose
Description

Betamethasone 10.6 mg IV Dose

Alias
UMLS CUI-1
C0005308
UMLS CUI-2
C0178602
Start Date and Time
Description

Betamethasone, Dosage, Start Date, Start time

Data type

datetime

Alias
UMLS CUI [1,1]
C0005308
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0808070
UMLS CUI [1,4]
C1301880
Stop Date and Time
Description

Betamethasone, Dosage, End Date, End time

Data type

datetime

Alias
UMLS CUI [1,1]
C0005308
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0806020
UMLS CUI [1,4]
C1522314
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Similar models

Investigational Product - IV Dosing

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
GSK221149A IV Dose - Rapid Infusion
C0304229 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
C0456962 (UMLS CUI-3)
Experimental drug, Dosage, Rapid, Start Date, Start time
Item
Start Date and Time
datetime
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0456962 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,4])
C1301880 (UMLS CUI [1,5])
Experimental drug, Dosage, Rapid, End Date, End time
Item
Stop Date and Time
datetime
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0456962 (UMLS CUI [1,3])
C0806020 (UMLS CUI [1,4])
C1522314 (UMLS CUI [1,5])
Item Group
GSK221149A IV Dose - Continuous (post rapid) infusion
C0304229 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
C0549178 (UMLS CUI-3)
Experimental drug, Dosage, Continuous, Start Date, Start time
Item
Start Date and Time
datetime
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,4])
C1301880 (UMLS CUI [1,5])
Experimental drug, Dosage, Continuous, End Date, End time
Item
Stop Date and Time
datetime
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,3])
C0806020 (UMLS CUI [1,4])
C1522314 (UMLS CUI [1,5])
Item Group
Betamethasone 10.6 mg IV Dose
C0005308 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
Betamethasone, Dosage, Start Date, Start time
Item
Start Date and Time
datetime
C0005308 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C1301880 (UMLS CUI [1,4])
Betamethasone, Dosage, End Date, End time
Item
Stop Date and Time
datetime
C0005308 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C1522314 (UMLS CUI [1,4])
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