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Clinical Trials/ACTRN12609000571279
ACTRN12609000571279CompletedPhase 3

Prospective non controlled study of immunogenicity of Human Papilloma Virus (HPV) Vaccine in groups at special risk of poor vaccine result

ational Health and Medical Research Council & Clinical Centre of Research Excellence(NHMRC CCRE) in Childhood and Adolescent Immunisation0 sites100 target enrollmentStarted: July 13, 2009Last updated:
Conditions

Trial Snapshot

Phase
Phase 3
Status
Completed
Sponsor
Enrollment
100

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Non-randomised trial
Primary Purpose
Prevention
Masking
Open (masking not used)

Eligibility Criteria

Ages
12 Years to 26 Years (—)
Sex
Female

Inclusion Criteria

  • Females aged 12-26 years
  • Have been diagnosed by a specialist with one of the six chronic medical conditions described.
  • Special Risk Groups
  • 1. Paediatric Rheumatalogical Disease
  • 2. Inflammatory Bowel Disease
  • 3. Acute Lymphoblastic Leukaemia
  • 4. Solid Organ Transplant Recipients (kidney and liver)
  • 5. Chronic Renal Disease
  • 6. Bone Marrow Transsplant

Exclusion Criteria

  • Previous immunisation with HPV vaccine
  • Recognised contraindication to the receipt of the vaccine e.g. anaphylaxis

Investigators

Sponsor
ational Health and Medical Research Council & Clinical Centre of Research Excellence(NHMRC CCRE) in Childhood and Adolescent Immunisation

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