ID

24566

Beschrijving

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

Trefwoorden

Versies (1)
  1. 06-08-17 06-08-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

6 augustus 2017

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

GSK Hepatitis A Vaccine Month 138 Visit 18 FOLLOW-UP STUDIES NCT00291876

Engels

GSK Hepatitis A Vaccine Month 138 FOLLOW-UP STUDIES NCT00291876

1 Formulieren  
Study administration
Beschrijving

Study administration

Center
Beschrijving

Center

Datatype

text

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

Date of Visit

Datatype

date

Alias
UMLS CUI [1]
C1320303
Subject Number
Beschrijving

Subject Identifier

Datatype

integer

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

FOLLOW-UP STUDIES

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

Follow Up Status

Datatype

boolean

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

adverse event

Datatype

text

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

other reason

Datatype

text

Alias
UMLS CUI [1]
C3840932
Terug naar het begin van de pagina

Similar models

GSK Hepatitis A Vaccine Month 138 FOLLOW-UP STUDIES NCT00291876

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

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