Randomized Study of Oral Contraceptives or Hormone Replacement Therapy in Women With Systemic Lupus Erythematosus

Systemic Lupus Erythematosus Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00006133
• Other study ID #: 199/15327
• Secondary ID: UAB-SELENA
• Status: Completed
• Phase: N/A
• First received: August 3, 2000
• Last updated: June 23, 2005
• Start date: June 2000

Study information

• Verified date: December 2003
• Source: National Center for Research Resources (NCRR)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

OBJECTIVES: I. Determine the effect of oral contraceptives containing low-dose synthetic estrogens and progestins on disease activity in premenopausal women with inactive, stable, or moderate systemic lupus erythematosus (SLE).

II. Determine the effect of hormone replacement therapy with conjugated estrogens and progestins on disease activity in postmenopausal women with inactive, stable, or moderate SLE.

Description:

PROTOCOL OUTLINE: This is a randomized, double-blind, placebo-controlled, multicenter study. Patients are stratified according to age/menopausal status (35 and under/premenopausal vs 50 and over/postmenopausal). Both strata are randomized to one of two treatment arms.

Stratum 1 (Premenopausal/Oral contraceptives): Patients receive either oral ethinyl estradiol and norethindrone or placebo daily for 28 days beginning on the Sunday following the first day of the menstrual cycle.

Stratum 2 (Postmenopausal/Hormone replacement therapy): Patients receive either oral estradiol and medroxyprogesterone or placebo on days 1-12 monthly.

Treatment continues in both arms of both strata for a total of 13 courses in the absence of a severe disease flare-up or other complication that would preclude further study participation.

All patients are followed at 1 year.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 970
• Accepts healthy volunteers: No
• Gender: Female
• Age group: N/A and older

Eligibility

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics--

Established systemic lupus erythematosus meeting American College of Rheumatology criteria

Inactive disease Systemic Lupus Erythematosus Activity Index (SLEDAI) score no greater than 4

No increase in score of more than 2 from baseline over the past 3 months

Receiving the equivalent of 5 mg or less of prednisone per day OR Stable/active disease SLEDAI score 5-12

No increase in score of more than 2 from baseline over the past 3 months

Prednisone dose up to 0.5 mg/kg/day for control of underlying disease allowed if stable dose for at least 3 weeks

No concurrent severe disease activity as defined by any of the following:

• Acute renal disease (i.e., rising creatinine levels, cellular sediment, or increasing proteinuria)

• Involvement of 3 or more organ systems requiring more than the equivalent of 0.5 mg/kg/day of prednisone

• Necessity of immediate hospitalization for symptom control

No presence of a high titer IgG, IgM, or IgA antiphospholipid antibodies (aPL) GPL and MPL no more than 40 APL no more than 50

No features of primary antiphospholipid antibody syndrome

--Prior/Concurrent Therapy--

Biologic therapy: Not specified

Chemotherapy: Not specified

Endocrine therapy: See Disease Characteristics

Radiotherapy: Not specified

Surgery: Prior hysterectomy allowed

--Patient Characteristics--

Age: 35 and under for oral contraceptive stratum (premenopausal) 50 and over for hormone replacement therapy stratum (postmenopausal)

Menopausal status:

• Premenopausal for oral contraceptive stratum

• Postmenopausal for hormone replacement therapy stratum

• Follicle-stimulating hormone greater than 40 mIU/mL OR Amenorrhea for 6 months

Performance status: See Disease Characteristics

Hematopoietic: Not specified

Hepatic:

• No hepatic dysfunction

• No tumors of the liver

Renal: See Disease Characteristics

Cardiovascular:

• No uncontrolled high blood pressure requiring frequent change in medication

• Concurrent hypertension controlled with stable medication allowed

• No history of spontaneous superficial or deep venous thrombosis or arterial thrombosis

• No prior myocardial infarction

• Oral contraceptive stratum: No angina No diastolic blood pressure greater than 90 mm Hg or systolic blood pressure greater than 140 mm Hg on 3 separate determinations

• Hormone replacement therapy stratum: No diastolic blood pressure greater than 95 mm Hg or systolic blood pressure greater than 145 mm Hg on 3 separate determinations

Pulmonary: No history of pulmonary embolus

Other:

• Not pregnant

• Oral contraceptive stratum: Negative pregnancy test Fertile patients must use effective barrier contraception

• No prior gynecologic malignancy or breast malignancy

• No undiagnosed vaginal bleeding

• No diabetes (present prior to use of glucocorticoids) requiring oral hypoglycemic medications or insulin

• No congenital hyperlipidemia

• No complicated migraines (i.e., associated with neurological sequelae)

Study Design

Allocation: Randomized, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Lupus Erythematosus, Systemic
• Systemic Lupus Erythematosus

Intervention

Drug:
• estradiol

• ethinyl estradiol

• medroxyprogesterone

• norethindrone

Locations

Country	Name	City	State
United States	University of Michigan Health Systems	Ann Arbor	Michigan
United States	Johns Hopkins University School of Medicine	Baltimore	Maryland
United States	University of Alabama Comprehensive Cancer Center	Birmingham	Alabama
United States	Montefiore Medical Center	Bronx	New York
United States	University of North Carolina	Chapel Hill	North Carolina
United States	Pritzker School of Medicine	Chicago	Illinois
United States	University of Texas- Houston Medical School	Houston	Texas
United States	University of California Los Angeles	Los Angeles	California
United States	Medical College of Wisconsin	Milwaukee	Wisconsin
United States	Hospital for Joint Diseases	New York	New York
United States	Hospital for Special Surgery	New York	New York
United States	Saint Luke's-Roosevelt Hospital Center	New York	New York
United States	University of Pennsylvania	Philadelphia	Pennsylvania
United States	University of Pittsburgh	Pittsburgh	Pennsylvania
United States	Rheumatology Associates of Long Island	Port Jefferson Station	New York
United States	University of California-San Francisco	San Francisco	California
United States	Louisiana State University School of Medicine	Shreveport	Louisiana

Sponsors (2)

Lead Sponsor	Collaborator
National Center for Research Resources (NCRR)	University of Alabama at Birmingham

Country where clinical trial is conducted

United States,