Overview

Immunogenicity and Safety of a Quadrivalent Human Papillomavirus (HPV) Vaccine in Patients With SLE: a Controlled Study

Status:
Completed
Trial end date:
2011-06-01
Target enrollment:
0
Participant gender:
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 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Tuen Mun Hospital
Treatments:
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