ID

38137

Descripción

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

Palabras clave

Versiones (1)
  1. 21/9/19 21/9/19 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

21 de septiembre de 2019

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

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

Inglés

Investigational Product - IV Dosing

1 formularios  
GSK221149A IV Dose - Rapid Infusion
Descripción

GSK221149A IV Dose - Rapid Infusion

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

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

Tipo de datos

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
Descripción

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

Tipo de datos

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
Descripción

GSK221149A IV Dose - Continuous (post rapid) infusion

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

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

Tipo de datos

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
Descripción

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

Tipo de datos

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
Descripción

Betamethasone 10.6 mg IV Dose

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

Betamethasone, Dosage, Start Date, Start time

Tipo de datos

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
Descripción

Betamethasone, Dosage, End Date, End time

Tipo de datos

datetime

Alias
UMLS CUI [1,1]
C0005308
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0806020
UMLS CUI [1,4]
C1522314
Volver a la parte superior de la página

Similar models

Investigational Product - IV Dosing

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial