Study genetic risk factors for antiphospholipid antibody syndrome
Part of Immune system & allergy clinical trials.
This study looks at genetic (inherited) risk factors in people who have antiphospholipid antibodies and related symptoms. Your results may help researchers better predict who is at risk and improve care for antiphospholipid antibody syndrome.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have antiphospholipid antibodies that are found in your blood more than once, at least 6 weeks apart
- Your antibody tests show medium or high anticardiolipin levels OR a positive lupus anticoagulant test both on repeat tests
- You also have symptoms that can happen with APS, such as blood clots or certain pregnancy problems
- If you do not fully meet the symptom criteria but you do have higher antibody levels, you may still join if you have close family members with APS
- You must have a documented antiphospholipid antibody finding (no antibody finding means you can’t enroll)
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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