Safety of Estrogens in Lupus: Hormone Replacement Therapy

Last updated: May 1, 2013
Sponsor: NYU Langone Health
Overall Status: Terminated

Phase

3

Condition

Cutaneous Lupus Erythematosus

Lupus

Musculoskeletal Diseases

Treatment

N/A

Clinical Study ID

NCT00000419
U01 AR42540 NIAMS-028A
U01AR042540
  • Ages 18-85
  • Female

Study Summary

Safety of Estrogens in Lupus Erythematosus - National Assessment (SELENA) is a study to test whether postmenopausal women with systemic lupus erythematosus (SLE, or lupus) can safely use the hormone estrogen. In this part of the study, we will look at the effects of estrogen replacement therapy on the activity and severity of disease in women with SLE.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Female

  • Unequivocal diagnosis of SLE

  • Inactive disease or stable on 0.5 mg/kg/day or less of prednisone

  • Chemical evidence of menopause or have stopped periods for at least 6 months

Exclusion

Exclusion Criteria:

  • 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

  • Gynecologic or breast cancer

  • Hepatic dysfunction or liver tumors

  • Diabetes mellitus (NOT due to steroids) with vascular disease

  • Congenital hyperlipidemia

  • Complicated migraine

  • Severe disease activity (SLEDAI >12)

  • Increase in SLEDAI >2 points in 3 months

  • Unexplained vaginal bleeding

  • Use of estrogen (HRT or OCP) for >1 month at any time after SLE diagnosis

  • FSH <40

  • Premenopausal myocardial infarction

Study Design

Total Participants: 350
Study Start date:
April 01, 1996
Estimated Completion Date:
August 31, 2002

Study Description

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 hormone replacement therapy (HRT) to women with SLE because of the widely held view that such treatment 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 HRT.

We will examine, in a multicenter, randomized, double-blind, placebo-controlled trial, the effect of hormonal replacement with conjugated estrogens on disease activity in postmenopausal women with SLE. We will recruit patients from clinics and private practices that include over 4,000 women with SLE, most belonging to minority groups.

We will give patients hormones for 1 year.

NOTE: This trial has been terminated as of August 2002 upon recommendation of the Data Safety Monitoring Board (DSMB), based on the findings of the WHI Trial. Study subjects have discontinued study drug but will continue followup visits to study doctors through May 2003

Connect with a study center

  • UAB Medical Center

    Birmingham, Alabama 35294
    United States

    Site Not Available

  • UCLA Medical Center, Dept. of Rheumatology

    Los Angeles, California 90024
    United States

    Site Not Available

  • University of Chicago Pritzker School of Medicine

    Chicago, Illinois 60637
    United States

    Site Not Available

  • Louisiana School of Medicine

    Shreveport, Louisiana 71130-3932
    United States

    Site Not Available

  • Johns Hopkins Hospital

    Baltimore, Maryland 21205
    United States

    Site Not Available

  • Univ. of Michigan Med. Ctr., Rheumatology Div.

    Ann Arbor, Michigan 48109-0358
    United States

    Site Not Available

  • Albert Einstein College of Medicine, Jacoby Hospital, Dept. of Rheumatology

    Bronx, New York 10461
    United States

    Site Not Available

  • Hospital for Joint Diseases

    New York, New York 10003
    United States

    Site Not Available

  • Hospital for Special Surgery

    New York, New York 10021
    United States

    Site Not Available

  • UNC Medical Center, Dept. of Rheumatology

    Chapel Hill, North Carolina 27599-7280
    United States

    Site Not Available

  • Oklahoma Medical Research Foundation

    Oklahoma City, Oklahoma 73104
    United States

    Site Not Available

  • Univ. of Pennsylvania Medical Center

    Philadelphia, Pennsylvania 19104
    United States

    Site Not Available

  • Univ. of Pittsburgh, Dept. of Rheumatology

    Pittsburgh, Pennsylvania 15213
    United States

    Site Not Available

  • University of Texas Health Sciences Center

    Houston, Texas 77030
    United States

    Site Not Available

  • Medical College of Virginia, Ambulatory Care Center

    Richmond, Virginia 23219
    United States

    Site Not Available

  • Medical College of Wisconsin

    Milwaukee, Wisconsin 53226
    United States

    Site Not Available

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