ID

37898

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

Mots-clés

Versions (1)
  1. 29/08/2019 29/08/2019 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

29 août 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
Modèle Commentaires :

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Betamethasone pharmacokinetics of a co-administered infusion of GSK221149A; 105036

Anglais

Status of Treatment Blind

1 Formulaires  
Status of Treatment Blind
Description

Status of Treatment Blind

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

Blinded Clinical Study, Status

Type de données

boolean

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

Subject Unblinding Event Record, Date in time, Time

Type de données

datetime

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

Subject Unblinding Event Record, Reason and justification

Type de données

text

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

Subject Unblinding Event Record, Reason and justification

Type de données

text

Alias
UMLS CUI [1,1]
C3897431
UMLS CUI [1,2]
C0566251
Retour au début de la page

Similar models

Status of Treatment Blind

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])
Retour au début de la page 

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