ID

14947

Description

This study will evaluate the safety, reactogenicity and immunogenicity of a booster dose of GSK Biologicals' pneumococcal conjugate vaccine compared to Prevenar™ given at 12-18 mo of age to children primed with either pneumococcal vaccine or Prevenar™ in study 105553. Antibody persistence will be evaluated at 8-14 mo after completion of the 3-dose immunization course in study 105553. The immune response to a booster dose of GSK Biologicals' pneumococcal conjugate vaccine will also be evaluated when given at 12-18 mo to subjects not primed with GSK Biologicals' vaccine but with Prevenar™. The study has 3 groups. 1 group of children primed with GSK Biologicals' pneumococcal conjugate vaccine will receive a booster dose of the same vaccine. 2nd group of children primed with Prevenar™ will receive a booster dose of Prevenar™ (control group). 3rd group of children primed with Prevenar™ will receive a booster dose of GSK Biologicals' pneumococcal conjugate vaccine. All children will receive concomitantly a booster dose of DTPa-HBV-IPV/Hib vaccine. NCT00370396 Part: Reason for non participation

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Versions (3)
  1. 09/05/2016 09/05/2016 -
  2. 10/05/2016 10/05/2016 -
  3. 10/05/2016 10/05/2016 - Julian Varghese
Téléchargé le

9 mai 2016

DOI

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Creative Commons BY-NC 3.0
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TEST StudyReason for non participation "Safety and Immunogenicity Study of a Booster Dose of GSK Biologicals' 10-valent Pneumococcal Conjugate Vaccine" NCT00370396

Anglais

Reason for non participation "Safety and Immunogenicity Study of a Booster Dose of GSK Biologicals' 10-valent Pneumococcal Conjugate Vaccine" NCT00370396

1 Formulaires  
Identification
Description

Identification

Alias
UMLS CUI-1
C1300638
Center number
Description

Center number

Type de données

text

Alias
UMLS CUI [1,1]
C1301943
UMLS CUI [1,2]
C0805701
Subject ID
Description

Subject ID

Type de données

text

Alias
UMLS CUI [1]
C2348585
Treatment Number
Description

Treatment Number

Type de données

text

Alias
UMLS CUI [1]
C1522541
Date of birth
Description

Date of birth

Type de données

date

Alias
UMLS CUI [1]
C0421451
Gender
Description

Gender

Type de données

text

Alias
UMLS CUI [1]
C0079399
Tracking Document Reason for non participation
Description

Tracking Document Reason for non participation

Alias
UMLS CUI-1
C0679823
UMLS CUI-2
C3166257
Previous subject number:
Description

Subject number

Type de données

text

Alias
UMLS CUI [1]
C1709561
Date of birth
Description

Date of birth

Type de données

date

Alias
UMLS CUI [1]
C0421451
Please document reason for non participation
Description

Please specify below

Type de données

integer

Alias
UMLS CUI [1]
C3166257
please specify criteria that are not fullfilled
Description

Specification of non-eligibility

Type de données

text

Alias
UMLS CUI [1]
C3166257
Retour au début de la page

Similar models

Reason for non participation "Safety and Immunogenicity Study of a Booster Dose of GSK Biologicals' 10-valent Pneumococcal Conjugate Vaccine" NCT00370396

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Identification
C1300638 (UMLS CUI-1)
Center number
Item
Center number
text
C1301943 (UMLS CUI [1,1])
C0805701 (UMLS CUI [1,2])
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Treatment Number
Item
Treatment Number
text
C1522541 (UMLS CUI [1])
Date of birth
Item
Date of birth
date
C0421451 (UMLS CUI [1])
Item
Gender
text
C0079399 (UMLS CUI [1])
Gender
Code List
Gender
CL Item
Male (m)
CL Item
Female (f)
Item Group
Tracking Document Reason for non participation
C0679823 (UMLS CUI-1)
C3166257 (UMLS CUI-2)
Subject number
Item
Previous subject number:
text
C1709561 (UMLS CUI [1])
Date of birth
Item
Date of birth
date
C0421451 (UMLS CUI [1])
Item
Please document reason for non participation
integer
C3166257 (UMLS CUI [1])
Reason for non participation
Code List
Please document reason for non participation
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 (3)
CL Item
Adverse events, or serious adverse event (4)
CL Item
Other (5)
CL Item
Subject died (6)
Specification of non-eligibility
Item
please specify criteria that are not fullfilled
text
C3166257 (UMLS CUI [1])
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