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Completed Not applicable Interventional

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

ClinicalTrials.gov ID: NCT00006133

Public ClinicalTrials.gov record NCT00006133. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 2:26 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT00006133
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
970 participants

Conditions and interventions

Eligibility (public fields only)

Age range
0 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 2000 (Type not available)
Primary completion
Not listed
Completion
Not listed
Last update posted
Jun 24, 2005

Started 2000

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
University of Alabama Comprehensive Cancer Center Birmingham Alabama 35294 —
University of California Los Angeles Los Angeles California 90095-6951 —
University of California-San Francisco San Francisco California 94143 —
Pritzker School of Medicine Chicago Illinois 60637 —
Louisiana State University School of Medicine Shreveport Louisiana 71130-3932 —
Johns Hopkins University School of Medicine Baltimore Maryland 21205 —
University of Michigan Health Systems Ann Arbor Michigan 48109 —
Hospital for Joint Diseases New York New York 10003 —
Saint Luke's-Roosevelt Hospital Center New York New York 10019 —
Hospital for Special Surgery New York New York 10021 —
Rheumatology Associates of Long Island Port Jefferson Station New York 11776 —
Montefiore Medical Center The Bronx New York 10467-2490 —
University of North Carolina Chapel Hill North Carolina 27599 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
University of Pittsburgh Pittsburgh Pennsylvania 15260 —
University of Texas- Houston Medical School Houston Texas 77030 —
Medical College of Wisconsin Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00006133, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 24, 2005 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00006133 live on ClinicalTrials.gov.

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