ID
35332
Description
Study ID: 101222 Clinical Study ID: 101222 Study Title: Study to demonstrate the non-inferiority of GSK Biologicals' DTPw-HBV/Hib Kft. vaccine compared to GSK Biologicals' Tritanrix™-HepB/Hiberix™ vaccine and to separate administration of DTPw-HBV Kft. and Hiberix™ vaccines with respect to the immunogenicity of all antigens, when administered to healthy infants. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: Combined Diphtheria, Tetanus, Whole Cell Pertussis, Hepatitis B, Haemophilus influenzae Type b Vaccine (KFT) Trade Name:Zilbrix/Hib Study Indication: Diphtheria; Haemophilus influenzae type b; Hepatitis B; Tetanus; Whole Cell Pertussis
Mots-clés
Versions (2)
- 27/02/2019 27/02/2019 -
- 28/02/2019 28/02/2019 -
Détendeur de droits
GSK group of companies
Téléchargé le
28 février 2019
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
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Immunogenicity of TPw-HBV/Hib Kft. Vaccine in healthy infants - 101222
VISIT 1 (Day 0 Birth)
- StudyEvent: ODM
Description
CONTRAINDICATIONS TO SUBSEQUENT VACCINATION
Description
The following adverse events (AEs) constitute absolute contraindications to further administration of the study vaccines; if any of these AEs occur during the study, the subject must not receive additional doses of vaccine but may continue other study procedures at the discretion of the investigator. The subject must be followed until resolution of the event, as with any AE :
Type de données
boolean
Description
hypersensitivity to vaccine
Type de données
boolean
Description
This is defined as an acute, severe central nervous system disorder occurring within 7 days following vaccination, and generally consisting of major alterations in consciousness, unresponsiveness, generalized or focal seizures that persist more than a few hours, with failure to recover within 24 hours. Even though causation by DTP vaccine cannot be established, no subsequent doses of pertussis vaccine should be given. In these circumstances the vaccination course should be continued with DT and HB vaccines.
Type de données
boolean
Description
The following AEs constitute contraindications to administration of the study vaccines at that point in time; if any one of these AEs occurs at the time scheduled for vaccination, the subject may be vaccinated at a later date, within the time window specified in the protocol, or withdrawn at the discretion of the investigator. The subject must be followed until resolution of the event, as with any AE.
Type de données
boolean
Description
Temperature
Type de données
boolean
Description
PRECAUTIONS
Description
If any of the following events occur in temporal relation to receipt of study vaccines, the decision to give subsequent doses of vaccine containing the pertussis component should be carefully considered.
Type de données
boolean
Description
Collapse or Shock
Type de données
boolean
Description
Crying
Type de données
boolean
Description
A history of febrile convulsions, a family history of convulsions, a family history of Sudden Infant Death Syndrome (SIDS) and a family history of an adverse event following TritanrixTM-HepB vaccination do not constitute contraindications.
Type de données
boolean
Description
Reminder
Type de données
text
Description
INFORMED CONSENT
Description
DEMOGRAPHICS
Description
Center number
Type de données
integer
Description
Date of birth
Type de données
date
Description
Gender
Type de données
text
Description
Race
Type de données
text
Description
ELIGIBILITY CHECK
Description
INCLUSION CRITERIA
Description
Tick the boxes corresponding to any of the inclusion criteria the subject failed
Type de données
boolean
Description
Tick the boxes corresponding to any of the inclusion criteria the subject failed
Type de données
boolean
Description
Tick the boxes corresponding to any of the inclusion criteria the subject failed
Type de données
boolean
Description
Tick the boxes corresponding to any of the inclusion criteria the subject failed
Type de données
boolean
Description
Tick the boxes corresponding to any of the inclusion criteria the subject failed
Type de données
boolean
Description
Tick the boxes corresponding to any of the inclusion criteria the subject failed
Type de données
boolean
Description
EXCLUSION CRITERIA
Description
Tick the box corresponding to any of the exclusion criteria that disqualified the subject from entry.
Type de données
boolean
Description
Tick the box corresponding to any of the exclusion criteria that disqualified the subject from entry.
Type de données
boolean
Description
Tick the box corresponding to any of the exclusion criteria that disqualified the subject from entry.
Type de données
boolean
Description
Tick the box corresponding to any of the exclusion criteria that disqualified the subject from entry.
Type de données
boolean
Description
Tick the box corresponding to any of the exclusion criteria that disqualified the subject from entry.
Type de données
boolean
Description
Tick the box corresponding to any of the exclusion criteria that disqualified the subject from entry.
Type de données
boolean
Description
Tick the box corresponding to any of the exclusion criteria that disqualified the subject from entry.
Type de données
boolean
Description
Tick the box corresponding to any of the exclusion criteria that disqualified the subject from entry.
Type de données
boolean
Description
Tick the box corresponding to any of the exclusion criteria that disqualified the subject from entry.
Type de données
boolean
Description
RANDOMISATION / TREATMENT ALLOCATION
Description
GROUP HBV AT BIRTH
Similar models
VISIT 1 (Day 0 Birth)
- StudyEvent: ODM