Lupus Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Women with lupus (SLE) who were under 40 years old when they started cyclophosphamide (CYC) treatment, and who did not receive a hormone-protecting injection called GnRH-a alongside it (Group 1)
- Women with lupus (SLE) who were under 40 years old when they started cyclophosphamide (CYC) treatment, and who did receive leuprolide acetate (a GnRH-a injection, given either monthly or every 3 months) alongside it (Group 2)
- Women with lupus (SLE) of a similar age who have never received cyclophosphamide (CYC) treatment, with or without GnRH-a, and who have no history of reproductive disorders, infertility, or untreated sexually transmitted infections (Control Group)
Who may not be able to join:
- Women who were 40 years old or older at the time cyclophosphamide (CYC) treatment began (applies to Groups 1 and 2)
- Women with a past or current history of reproductive disorders, infertility, or untreated sexually transmitted infections (applies to all groups)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Sarfaraz A Hasni, M.D., National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Phone: (301) 451-1599
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
POI
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.