Completed

Safety of Estrogens in Lupus Erythematosus - National Assessment (SELENA): Oral Contraceptives

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What is being tested

Data Collection

Who is being recruted

Autoimmune Diseases+2

+ Connective Tissue Diseases

+ Immune System Diseases

From 18 to 39 Years
+21 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Phase 3
Interventional
Study Start: June 1997
See protocol details

Summary

Principal SponsorNYU Langone Health
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: June 1, 1997

Actual date on which the first participant was enrolled.

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.

Official TitleSafety of Estrogens in Lupus Erythematosus - National Assessment (SELENA): Oral Contraceptives
NCT00000420
Principal SponsorNYU Langone Health
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

350 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Female

Biological sex of participants that are eligible to enroll.

From 18 to 39 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Autoimmune DiseasesConnective Tissue DiseasesImmune System DiseasesLupus Erythematosus, SystemicSkin and Connective Tissue Diseases

Criteria

5 inclusion criteria required to participate
Female

Unequivocal diagnosis of SLE

Inactive disease or be stable on 0.5 mg/kg/day or less of predisone

Must be between 18 and 39 years old if non-smoker

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16 exclusion criteria prevent from participating
Blood pressure >145/95 on three occasions

Deep vein, arterial thrombosis or pulmonary embolus

GPL >40; MPL >40; APL >50; dRVVT >37 sec

APL antibody syndrome ever

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Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 15 locations

Suspended

UCLA Medical Center, Dept. of Rheumatology

Los Angeles, United StatesOpen UCLA Medical Center, Dept. of Rheumatology in Google Maps
Suspended

University of Chicago Pritzker School of Medicine

Chicago, United States
Suspended

Louisiana School of Medicine, Dept. of Medicine/Immunology

Shreveport, United States
Suspended

Johns Hopkins Hospital, Dept. of Rheumatology

Baltimore, United States
Completed15 Study Centers