ID

37898

Beskrivning

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

Nyckelord

Versioner (1)
  1. 2019-08-29 2019-08-29 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

29 augusti 2019

DOI

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Licens

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

Engelsk

Status of Treatment Blind

1 Formulär  
Status of Treatment Blind
Beskrivning

Status of Treatment Blind

Alias
UMLS CUI-1
C2347038
UMLS CUI-2
C0449438
Was the treatment blind broken during the study?
Beskrivning

Blinded Clinical Study, Status

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2347038
UMLS CUI [1,2]
C0449438
If Yes, Date/time blind broken
Beskrivning

Subject Unblinding Event Record, Date in time, Time

Datatyp

datetime

Alias
UMLS CUI [1,1]
C3897431
UMLS CUI [1,2]
C0011008
UMLS CUI [1,3]
C0040223
If Yes, Reason blind broken
Beskrivning

Subject Unblinding Event Record, Reason and justification

Datatyp

text

Alias
UMLS CUI [1,1]
C3897431
UMLS CUI [1,2]
C0566251
Specify
Beskrivning

Subject Unblinding Event Record, Reason and justification

Datatyp

text

Alias
UMLS CUI [1,1]
C3897431
UMLS CUI [1,2]
C0566251
Tillbaka till toppen

Similar models

Status of Treatment Blind

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Status of Treatment Blind
C2347038 (UMLS CUI-1)
C0449438 (UMLS CUI-2)
Blinded Clinical Study, Status
Item
Was the treatment blind broken during the study?
boolean
C2347038 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
Subject Unblinding Event Record, Date in time, Time
Item
If Yes, Date/time blind broken
datetime
C3897431 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Item
If Yes, Reason blind broken
text
C3897431 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])
Subject Unblinding Event Record, Reason and justification
Code List
If Yes, Reason blind broken
CL Item
Medical emergency requiring identification of investigational product for further treatment (1)
CL Item
Other, specify (2)
Subject Unblinding Event Record, Reason and justification
Item
Specify
text
C3897431 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])
Tillbaka till toppen 

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