Phase 3 Uveitis Trial, Not Yet 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:
- You are between 18 and 50 years old.
- You have been diagnosed with Behçet's Disease using the standard international diagnostic criteria (ISG criteria).
- You have not previously had blood vessel complications from Behçet's Disease, or you have not been treated with immune-suppressing medicines for blood vessel complications.
- You have been diagnosed with a blood clot in a vein in your leg or lower body within the last 14 days before joining the study.
- Your blood clot has been confirmed by ultrasound, a special X-ray (venography), CT scan, or MRI scan showing specific signs of a clot.
- If you are a woman who could become pregnant, you must not be pregnant or breastfeeding, and you must be using effective birth control, be past menopause (no periods for at least 1 year), or have had a surgical procedure to prevent pregnancy.
- You are able to give written consent and follow the study's requirements.
Who may not be able to join:
- You have any abnormal bulging of a blood vessel (aneurysm) anywhere in your body.
- You have another serious long-term illness besides Behçet's Disease.
- You have previously had a bad reaction or intolerance to the medication Rivaroxaban.
- You have taken immune-suppressing medicines (such as azathioprine, cyclosporine, or certain biological medicines) within the last 6 months.
- You have taken steroid medicines (such as cortisone) for more than 3 months for Behçet's Disease skin or mouth symptoms.
- You have already received blood-thinning injections (such as heparin) for more than 48 hours, or more than one dose of warfarin-type medicines, before joining the study.
- You have already had a procedure to remove the clot, a filter placed in a large vein, or clot-dissolving treatment for your current clot.
- You are planning to receive a live vaccine within 30 days of joining the study.
- You have a significant uncontrolled illness affecting the heart, lungs, liver, kidneys, blood, gut, nerves, or an active infection or cancer that could affect the study results.
- You are due to have surgery or have another medical condition that the study doctor feels makes you unsuitable for the trial.
- You have had cancer in the last 5 years (with some exceptions for certain minor skin cancers or early-stage cervical changes — confirm with trial site).
- Your kidneys are not working well enough (confirmed by a blood test showing low kidney filtration rate below 30 ml/min).
- You have serious liver disease, such as hepatitis or cirrhosis, or abnormal liver blood test results.
- You are actively bleeding or are at high risk of bleeding, which would make blood-thinning treatment unsafe for you.
- Your blood pressure is very high and not under control (above 180/110 mmHg).
- You have severe anaemia (low red blood cell levels, confirmed by a blood test).
- You are pregnant, breastfeeding, or a woman of childbearing age not using contraception.
- You are taking certain strong medications that affect how the body processes Rivaroxaban (such as some HIV medicines, systemic ketoconazole, rifampin, carbamazepine, or phenytoin).
- You have taken part in another clinical drug trial within the last 30 days.
- Your life expectancy is less than 3 months.
- You have had a serious infection in the last 60 days, such as a heart valve infection, tuberculosis, or other opportunistic infections.
- You are currently misusing alcohol or substances, or have had a substance dependence problem within the last year.
- You have tested positive for Hepatitis B, Hepatitis C, or HIV.
- You have a known blood clotting disorder or significant abnormal blood test results (confirm with trial site).
- You have had suicidal behaviour in the last 6 months, or have had serious thoughts of suicide in the last 2 months (confirm with trial site).
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: Fatma Alibaz-Oner, Prof, Marmara University
Phone: +90 216 625 45 45
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
Rate of Thrombotic Relapse at 52 Weeks
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.