Predictors of Pregnancy Outcome in Systemic Lupus Erythematosus (SLE) and Antiphospholipid Syndrome (APS)
Recruiting now NCT00198068
Run by Hospital for Special Surgery, New York · for 18 to 45 · Women · accepts healthy volunteers
What this study is about
The PROMISSE Study is an observational study of 700 pregnant patients, enrolled at nine major clinical centers. The purpose of the study is 1) to determine whether certain proteins (called complement split products) that can injure healthy organs can be used to predict poor pregnancy outcome in patients with systemic lupus erythematosus (SLE) and anti-phospholipid syndrome (APS), and/or 2) to determine whether elevated levels of circulating antiangiogenic factors predict pregnancy complications in patients with aPL antibodies and/or SLE.
Who can join (things the study team will check)
✅ You may be able to join if…
- Patient pregnant with live intrauterine pregnancy, as defined by positive test for elevated β-HCG, but ≤ 12 weeks by gestation (for subjects without aPL antibodies) and ≤18 weeks (for subjects with aPL antibodies)
- Patient between the ages of 18-45 and able to give informed consent, or age < 18 years with parental consent
- Hematocrit > 26%
- For APL positive:
- aCL: IgG >= 40 GPL units; IgM >= 40 MPL units
- Positive LAC (RVVT, Kaolin, dilute TTI or PTT LA)
- Anti-β2GPI: IgG >= 40 GPL units; IgM >= 40 MPL units
- For control subjects:
- At least one successful pregnancy
- No history of fetal death (death of conceptus ≥ 10 weeks' gestation)
- No more than 1 miscarriage < 10 weeks' gestation
- No history of positive aPL in local lab or positive aPL in core labs at screening
- Not currently a smoker
- No medical problems requiring chronic treatment
🚫 You may not be able to join if…
- Diabetes mellitus (Type I and Type II) antedating pregnancy
- Known or suspected hereditary complement deficiency (defined by CH50 = 0)
Where this trial is running
- Northwestern University, Chicago, Illinois, United States
- University of Chicago, Chicago, Illinois, United States
- Johns Hopkins Hospital, Baltimore, Maryland, United States
- NYU Langone Medical Center/Hospital for Joint Diseases, New York, New York, United States
- Hospital for Special Surgery, New York, New York, United States
- Columbia University Medical Center, New York, New York, United States
- Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, United States
- University of Utah Salt Lake City, Salt Lake City, Utah, United States
- Mt. Sinai Hospital, Toronto, Ontario, Canada
- Guy's & St Thomas' NHS Foundation Trust, London, United Kingdom
Who to contact
Marta M. Guerra, MS · 212-774-7361 · guerram@hss.edu
It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT00198068.
Verify everything on the official ClinicalTrials.gov record. Page updated July 2026.