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

Primary Purpose

Systemic Lupus Erythematosus

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
estradiol
ethinyl estradiol
medroxyprogesterone
norethindrone
Sponsored by
National Center for Research Resources (NCRR)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Systemic Lupus Erythematosus focused on measuring arthritis & connective tissue diseases, immunologic disorders and infectious disorders, rare disease, systemic lupus erythematosus

Eligibility Criteria

0 Years - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

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)

Sites / Locations

  • University of Alabama Comprehensive Cancer Center
  • University of California Los Angeles
  • University of California-San Francisco
  • Pritzker School of Medicine
  • Louisiana State University School of Medicine
  • Johns Hopkins University School of Medicine
  • University of Michigan Health Systems
  • Montefiore Medical Center
  • Hospital for Joint Diseases
  • Saint Luke's-Roosevelt Hospital Center
  • Hospital for Special Surgery
  • Rheumatology Associates of Long Island
  • University of North Carolina
  • University of Pennsylvania
  • University of Pittsburgh
  • University of Texas- Houston Medical School
  • Medical College of Wisconsin

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
August 3, 2000
Last Updated
June 23, 2005
Sponsor
National Center for Research Resources (NCRR)
Collaborators
University of Alabama at Birmingham
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1. Study Identification

Unique Protocol Identification Number
NCT00006133
Brief Title
Randomized Study of Oral Contraceptives or Hormone Replacement Therapy in Women With Systemic Lupus Erythematosus
Study Type
Interventional

2. Study Status

Record Verification Date
December 2003
Overall Recruitment Status
Completed
Study Start Date
June 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
National Center for Research Resources (NCRR)
Collaborators
University of Alabama at Birmingham

4. Oversight

5. Study Description

Brief 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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Systemic Lupus Erythematosus
Keywords
arthritis & connective tissue diseases, immunologic disorders and infectious disorders, rare disease, systemic lupus erythematosus

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Masking
Double
Allocation
Randomized
Enrollment
970 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
estradiol
Intervention Type
Drug
Intervention Name(s)
ethinyl estradiol
Intervention Type
Drug
Intervention Name(s)
medroxyprogesterone
Intervention Type
Drug
Intervention Name(s)
norethindrone

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
0 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Graciela S. Alarcon
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Study Chair
Facility Information:
Facility Name
University of Alabama Comprehensive Cancer Center
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35294
Country
United States
Facility Name
University of California Los Angeles
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095-6951
Country
United States
Facility Name
University of California-San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Facility Name
Pritzker School of Medicine
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60637
Country
United States
Facility Name
Louisiana State University School of Medicine
City
Shreveport
State/Province
Louisiana
ZIP/Postal Code
71130-3932
Country
United States
Facility Name
Johns Hopkins University School of Medicine
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21205
Country
United States
Facility Name
University of Michigan Health Systems
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States
Facility Name
Montefiore Medical Center
City
Bronx
State/Province
New York
ZIP/Postal Code
10467-2490
Country
United States
Facility Name
Hospital for Joint Diseases
City
New York
State/Province
New York
ZIP/Postal Code
10003
Country
United States
Facility Name
Saint Luke's-Roosevelt Hospital Center
City
New York
State/Province
New York
ZIP/Postal Code
10019
Country
United States
Facility Name
Hospital for Special Surgery
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
Facility Name
Rheumatology Associates of Long Island
City
Port Jefferson Station
State/Province
New York
ZIP/Postal Code
11776
Country
United States
Facility Name
University of North Carolina
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
Facility Name
University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
University of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15260
Country
United States
Facility Name
University of Texas- Houston Medical School
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
Medical College of Wisconsin
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53226
Country
United States

12. IPD Sharing Statement

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

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