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Safety of Estrogens in Lupus: Hormone Replacement Therapy

Phase 3
Terminated
Conditions
Systemic Lupus Erythematosus
Registration Number
NCT00000419
Lead Sponsor
NYU Langone Health
Brief 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.

Detailed 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

Recruitment & Eligibility

Status
TERMINATED
Sex
Female
Target Recruitment
350
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 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

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (16)

Johns Hopkins Hospital

🇺🇸

Baltimore, Maryland, United States

University of Chicago Pritzker School of Medicine

🇺🇸

Chicago, Illinois, United States

Univ. of Pittsburgh, Dept. of Rheumatology

🇺🇸

Pittsburgh, Pennsylvania, United States

UAB Medical Center

🇺🇸

Birmingham, Alabama, United States

Oklahoma Medical Research Foundation

🇺🇸

Oklahoma City, Oklahoma, United States

University of Texas Health Sciences Center

🇺🇸

Houston, Texas, United States

UCLA Medical Center, Dept. of Rheumatology

🇺🇸

Los Angeles, California, United States

Louisiana School of Medicine

🇺🇸

Shreveport, Louisiana, United States

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

🇺🇸

Bronx, New York, United States

Hospital for Special Surgery

🇺🇸

New York, New York, United States

Hospital for Joint Diseases

🇺🇸

New York, New York, United States

Univ. of Pennsylvania Medical Center

🇺🇸

Philadelphia, Pennsylvania, United States

UNC Medical Center, Dept. of Rheumatology

🇺🇸

Chapel Hill, North Carolina, United States

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

🇺🇸

Ann Arbor, Michigan, United States

Medical College of Virginia, Ambulatory Care Center

🇺🇸

Richmond, Virginia, United States

Medical College of Wisconsin

🇺🇸

Milwaukee, Wisconsin, United States

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