Safety of Estrogens in Lupus Erythematosus - National Assessment (SELENA) is a study to test whether women with systemic lupus erythematosus (SLE or lupus) can safely use estrogen. We will determine this by looking at the effects of oral contraceptives (birth control pills, also known as "the pill") on disease activity and severity in women with SLE. The results of the study will show whether it is safe for women with SLE to use the pill.
This study tests the effect of exogenous female hormones on disease activity and severity in women with systemic lupus erythematosus (SLE). Physicians generally do not prescribe oral contraceptives (OCs) to women with lupus because of the widely held view that these drugs can activate SLE. This practice is based on the greater incidence of SLE in women than in men, biologic abnormalities of estrogen metabolism, murine models of lupus, several anecdotes of patients having disease flares while receiving exogenous hormones, and a single retrospective study in patients with preexisting renal disease. By contrast, recent retrospective studies suggest that the rate of flare is not significantly increased in patients taking OCs. The preexisting data is insufficient to warrant the dismissal of a potentially important birth control option in a disease that predominantly affects women in their reproductive years and whose fertility is not altered by the disease. Moreover, the use of OCs to preserve fertility in patients taking cyclophosphamide and the use of estrogens to prevent coronary artery disease and postmenopausal and steroid-induced osteoporosis are timely considerations. We will attempt to define, in a multicenter, randomized, double-blind, placebo-controlled trial, the effect of OCs containing low-dose synthetic estrogens and progestins on disease activity in women with SLE. Because the research hypothesis is that OCs do not increase the risk of flares, we have designed the study to be able to detect minimal increases in the rate of flares in patients taking OCs. We will enroll patients with inactive, stable, or moderate disease requiring less than 0.5 mg prednisone per kg of bodyweight per day over a 2-year period and randomize them to receive birth control pills or placebo pills for 12 months. During that time, the patient must use condoms or a diaphragm as birth control. We will recruit patients from clinics and private practices that include over 4,000 women with SLE, most belonging to minority groups.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
350
UCLA Medical Center, Dept. of Rheumatology
Los Angeles, California, United States
University of Chicago Pritzker School of Medicine
Chicago, Illinois, United States
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Louisiana School of Medicine, Dept. of Medicine/Immunology
Shreveport, Louisiana, United States
Johns Hopkins Hospital, Dept. of Rheumatology
Baltimore, Maryland, United States
Univ. of Michigan Med. Ctr., Rheumatology Division
Ann Arbor, Michigan, United States
Hospital for Joint Diseases
New York, New York, United States
Hospital for Special Surgery, Dept. of Rheumatology
New York, New York, United States
Albert Einstein College of Medicine, Jacobi Hospital, Dept. of Rheumatology
The Bronx, New York, United States
UNC Medical Center, Dept. of Rheumatology
Chapel Hill, North Carolina, United States
Oklahoma Medical Research Foundation
Oklahoma City, Oklahoma, United States
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