ID

29436

Description

Tracking Document Long Term Follow-up Study ID: 101695 Ext. Mth30 Clinical Study ID: 101695 Study Title: Long-term study of immune response persistence of GSK Biologicals' 2-dose thiomersal-free Engerix™-B and 3-dose preservative-free Engerix™-B vaccines in subjects aged 11-15 yrs Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00343915 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: Hepatitis B Vaccine, Recombinant Trade Name: BIO HBV; Engerix-B Study Indication: Hepatitis B

Mots-clés

Versions (1)
  1. 24/03/2018 24/03/2018 -
Détendeur de droits

GlaxoSmithKline (GSK)

Téléchargé le

24 mars 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
Modèle Commentaires :

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GSK Biologicals' 2-dose thiomersal-free Engerix™-B and 3-dose preservative-free Engerix™-B vaccines Study ID: 101695 NCT00343915

Anglais

Tracking Document Long Term Follow-up

1 Formulaires  
Tracking Document Safety Follow-Up
Description

Tracking Document Safety Follow-Up

Alias
UMLS CUI-1
C3889409
Subject number of previous study
Description

Subject number

Type de données

integer

Alias
UMLS CUI [1]
C2348585
Subject initials first name family name
Description

Subject initials

Type de données

text

Alias
UMLS CUI [1,1]
C1997894
UMLS CUI [1,2]
C2986440
Date of birth (day month year)
Description

Date of birth

Type de données

date

Alias
UMLS CUI [1]
C0421451
Please contact the following subjects for inclusion in the long-term follow-up study and document whether or not he/she agrees to participate.
Description

Follow-up Participation

Type de données

integer

Alias
UMLS CUI [1,1]
C0016441
UMLS CUI [1,2]
C2348568
Date of Contact
Description

Date of Contact

Type de données

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C1705415
Administrative documentation
Description

Administrative documentation

Alias
UMLS CUI-1
C1320722
Investigator signature:
Description

Signature

Type de données

text

Alias
UMLS CUI [1]
C2346576
Investigator name
Description

Name of Investigator

Type de données

text

Alias
UMLS CUI [1]
C2826892
Date
Description

Date

Type de données

date

Alias
UMLS CUI [1,1]
C2346576
UMLS CUI [1,2]
C0011008
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Similar models

Tracking Document Long Term Follow-up

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Tracking Document Safety Follow-Up
C3889409 (UMLS CUI-1)
Subject number
Item
Subject number of previous study
integer
C2348585 (UMLS CUI [1])
Subject initials
Item
Subject initials first name family name
text
C1997894 (UMLS CUI [1,1])
C2986440 (UMLS CUI [1,2])
Date of birth
Item
Date of birth (day month year)
date
C0421451 (UMLS CUI [1])
Item
Please contact the following subjects for inclusion in the long-term follow-up study and document whether or not he/she agrees to participate.
integer
C0016441 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
SAE(s)
Code List
Please contact the following subjects for inclusion in the long-term follow-up study and document whether or not he/she agrees to participate.
CL Item
Subject not eligible (1)
CL Item
Subject lost to follow-up or not reached (2)
CL Item
Subject eligible but not willing to participate due to: adverse events, or serious adverse event: (3)
CL Item
please specify: ____________________ (4)
CL Item
other: please specify: ____________________ (5)
CL Item
Subject eligible and agreed to participate in the long-term follow-up study (4)
Date of Contact
Item
Date of Contact
date
C0011008 (UMLS CUI [1,1])
C1705415 (UMLS CUI [1,2])
Item Group
Administrative documentation
C1320722 (UMLS CUI-1)
Signature
Item
Investigator signature:
text
C2346576 (UMLS CUI [1])
Name of Investigator
Item
Investigator name
text
C2826892 (UMLS CUI [1])
Date
Item
Date
date
C2346576 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Retour au début de la page 

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