Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Chicago, Illinois 60637


Purpose:

The purpose of this study is to evaluate the immunogenicity and safety of the HPV vaccine Gardasil in young women.


Study summary:

Female patients with systemic lupus erythematosus (SLE) have been found have higher rates of persistent HPV infections and precancerous lesions compared to the healthy population. The HPV vaccine Gardasil has been found to be safe and efficacious in females aged 9 to 26 years. There are no data on the immunogenicity and safety of Gardasil in females with SLE. Immune dysfunction related to SLE itself and the immunosuppression secondary to treatment of SLE might prevent patients with SLE from developing an adequate immune response to the vaccine. Also, theoretically, the vaccine might induce a disease exacerbation or production of new autoantibodies. The purpose of this study is to evaluate immunogenicity and safety of Gardasil and its effects on autoantibody profile in female SLE patients aged 9-26 years


Criteria:

Inclusion Criteria: - Age: 9 to 26 years of age - Gender: Female - All patients must fulfill the revised American College of Rheumatology Classification Criteria for SLE diagnosis. - Current SLEDAI score ≤ 6 - Written, witnessed informed consent and/or assent will be obtained from the subject and the subject's parents (if under 18 years of age) or legally acceptable representative prior to enrollment Exclusion Criteria: - Acute exacerbation of disease within past 30 days which required increase in corticosteroid dose, initiation of a new immunosuppressive medication, or hospitalization - Current SLEDAI score > 6 - Patients who have received rituximab in the last 6 months, or are currently on cyclophosphamide treatment - History of allergic disease or reactions likely to be exacerbated by any component of the study vaccine - Previous administration of any HPV vaccine


NCT ID:

NCT00786409


Primary Contact:

Principal Investigator
Linda Wagner-Weiner, MD
University of Chicago


Backup Contact:

N/A


Location Contact:

Chicago, Illinois 60637
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.