Overview
Immunogenicity and Safety of a Quadrivalent Human Papillomavirus (HPV) Vaccine in Patients With SLE: a Controlled Study
Status:
Completed
Completed
Trial end date:
2011-06-01
2011-06-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The purpose of this trial is to study the effect of Human Papillomavirus (HPV) vaccination on the elevation of antibody titer to 4 serotypes of HPV in patients with systemic lupus erythematous and compare the antibody response with an equal number of age-matched healthy women.Phase:
Phase 4Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Tuen Mun HospitalTreatments:
Vaccines
Criteria
Inclusion Criteria:SLE patients
- Female patients aged ≤ 35 years
- Fulfilling the American College of Rheumatology (ACR) criteria for the classification
of SLE
- Having received a stable dose of prednisolone and/or other immunosuppressive agents
within 3 months of study entry
- Able to give written informed consent
Controls
- Women aged ≤ 35 years, matched those of SLE patients recruited
- No known chronic medical diseases
- Not receiving any long-term medications including herbs
Exclusion Criteria:
- History of allergy to HPV vaccines