ID

24566

Descripción

Study ID: 100571 (M138) Clinical Study ID: 100571 Study Title: Double-blind randomized study to evaluate the immunogenicity and reactogenicity of two different lots of GlaxoSmithKline Biologicals' inactivated hepatitis A vaccine containing 1440 EL.U of antigen per mL and injected according to a 0, 12 month schedule in healthy adult volunteers Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00291876 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 4 Study Recruitment Status: Completed Generic Name: Hepatitis A Vaccine, Inactivated Trade Name: Havrix Study Indication: Hepatitis A https://clinicaltrials.gov/ct2/show/NCT00291876

Link

https://clinicaltrials.gov/ct2/show/NCT00291876

Palabras clave

Versiones (1)
  1. 6/8/17 6/8/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

6 de agosto de 2017

DOI

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Licencia

Creative Commons BY-NC 3.0
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GSK Hepatitis A Vaccine Month 138 Visit 18 FOLLOW-UP STUDIES NCT00291876

Inglés

GSK Hepatitis A Vaccine Month 138 FOLLOW-UP STUDIES NCT00291876

1 formularios  
Study administration
Descripción

Study administration

Center
Descripción

Center

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1301943
UMLS CUI [1,2]
C0600091
Date of Visit
Descripción

Date of Visit

Tipo de datos

date

Alias
UMLS CUI [1]
C1320303
Subject Number
Descripción

Subject Identifier

Tipo de datos

integer

Alias
UMLS CUI [1]
C2348585
FOLLOW-UP STUDIES
Descripción

FOLLOW-UP STUDIES

Would the subject be willing to participate in a follow-up study?
Descripción

Follow Up Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0589120
If No, please specify reason: Adverse Events, or Serious Adverse Events: please specify:
Descripción

adverse event

Tipo de datos

text

Alias
UMLS CUI [1]
C0877248
If No, please specify reason: Other: please specify:
Descripción

other reason

Tipo de datos

text

Alias
UMLS CUI [1]
C3840932
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Similar models

GSK Hepatitis A Vaccine Month 138 FOLLOW-UP STUDIES NCT00291876

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Study administration
Center
Item
Center
text
C1301943 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Date of Visit
Item
Date of Visit
date
C1320303 (UMLS CUI [1])
Subject Identifier
Item
Subject Number
integer
C2348585 (UMLS CUI [1])
Item Group
FOLLOW-UP STUDIES
Follow Up Status
Item
Would the subject be willing to participate in a follow-up study?
boolean
C0589120 (UMLS CUI [1])
adverse event
Item
If No, please specify reason: Adverse Events, or Serious Adverse Events: please specify:
text
C0877248 (UMLS CUI [1])
other reason
Item
If No, please specify reason: Other: please specify:
text
C3840932 (UMLS CUI [1])
Volver a la parte superior de la página 

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