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| Sponsor: | National Center for Research Resources (NCRR) |
|---|---|
| Collaborator: |
University of Alabama at Birmingham |
| Information provided by: | National Center for Research Resources (NCRR) |
| ClinicalTrials.gov Identifier: | NCT00006133 |
Purpose
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.
| Condition | Intervention |
|---|---|
|
Systemic Lupus Erythematosus |
Drug: estradiol Drug: ethinyl estradiol Drug: medroxyprogesterone Drug: norethindrone |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Placebo Control |
| Estimated Enrollment: | 970 |
| Study Start Date: | June 2000 |
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.
Eligibility| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
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:
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:
Performance status: See Disease Characteristics
Hematopoietic: Not specified
Hepatic:
Renal: See Disease Characteristics
Cardiovascular:
Pulmonary: No history of pulmonary embolus
Other:
Contacts and Locations| United States, Alabama | |
| University of Alabama Comprehensive Cancer Center | |
| Birmingham, Alabama, United States, 35294 | |
| United States, California | |
| University of California Los Angeles | |
| Los Angeles, California, United States, 90095-6951 | |
| University of California-San Francisco | |
| San Francisco, California, United States, 94143 | |
| United States, Illinois | |
| Pritzker School of Medicine | |
| Chicago, Illinois, United States, 60637 | |
| United States, Louisiana | |
| Louisiana State University School of Medicine | |
| Shreveport, Louisiana, United States, 71130-3932 | |
| United States, Maryland | |
| Johns Hopkins University School of Medicine | |
| Baltimore, Maryland, United States, 21205 | |
| United States, Michigan | |
| University of Michigan Health Systems | |
| Ann Arbor, Michigan, United States, 48109 | |
| United States, New York | |
| Hospital for Joint Diseases | |
| New York, New York, United States, 10003 | |
| Hospital for Special Surgery | |
| New York, New York, United States, 10021 | |
| Montefiore Medical Center | |
| Bronx, New York, United States, 10467-2490 | |
| Rheumatology Associates of Long Island | |
| Port Jefferson Station, New York, United States, 11776 | |
| Saint Luke's-Roosevelt Hospital Center | |
| New York, New York, United States, 10019 | |
| United States, North Carolina | |
| University of North Carolina | |
| Chapel Hill, North Carolina, United States, 27599 | |
| United States, Pennsylvania | |
| University of Pennsylvania | |
| Philadelphia, Pennsylvania, United States, 19104 | |
| University of Pittsburgh | |
| Pittsburgh, Pennsylvania, United States, 15260 | |
| United States, Texas | |
| University of Texas- Houston Medical School | |
| Houston, Texas, United States, 77030 | |
| United States, Wisconsin | |
| Medical College of Wisconsin | |
| Milwaukee, Wisconsin, United States, 53226 | |
| Study Chair: | Graciela S. Alarcon | University of Alabama at Birmingham |
More Information
| Study ID Numbers: | 199/15327, UAB-SELENA |
| Study First Received: | August 3, 2000 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00006133 History of Changes |
| Health Authority: | United States: Federal Government |
|
arthritis & connective tissue diseases immunologic disorders and infectious disorders rare disease systemic lupus erythematosus |
|
Medroxyprogesterone 17-Acetate Antineoplastic Agents Contraceptive Agents Estradiol valerate Contraceptives, Oral Physiological Effects of Drugs Contraceptive Agents, Female Hormones, Hormone Substitutes, and Hormone Antagonists Estradiol 17 beta-cypionate Reproductive Control Agents Contraceptive Agents, Male Hormones Lupus Erythematosus, Systemic Norethindrone |
Estradiol 3-benzoate Therapeutic Uses Connective Tissue Diseases Contraceptives, Oral, Synthetic Polyestradiol phosphate Estrogens Autoimmune Diseases Antineoplastic Agents, Hormonal Immune System Diseases Ethinyl Estradiol Estradiol Pharmacologic Actions Medroxyprogesterone Norethindrone acetate |