Ireland
--:--IST
Starting soon Observational

Cangrelor As Treatment for Cardiac Surgery Associated With Heparin Induced Thrombocytopenia

NCT07817680 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-11-01
Last updated
2026-09-14

Condition(s) studied

Heparin-induced Thrombocytopenia

Study summary

Heparin-induced thrombocytopenia (HIT) is a rare but serious immune complication of heparin exposure that paradoxically increases the risk of thrombosis. In patients undergoing cardiac surgery with cardiopulmonary bypass (CPB), heparin is essential to prevent circuit clotting, yet contraindicated in HIT. Available alternatives carry significant limitations. Cangrelor, an intravenous reversible P2Y12 inhibitor, has shown promise in case reports and small series in this context, but no multicenter study exists. CATCH-IT is a multicenter retrospective observational study conducted across 11 French cardiac surgery centers, aiming to describe the safety and efficacy of cangrelor combined with heparin during CPB in confirmed HIT patients, by estimating the incidence of major bleeding and thrombotic events within 7 days after surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 years * Confirmed or highly probable HIT: 4T score ≥ 3 AND positive anti-PF4 antibodies (ELISA or equivalent), and when available, positive functional platelet test * Cardiac or aortic surgery with cardiopulmonary bypass (CPB) * Cangrelor administered in the perioperative period * No objection to use of medical data Exclusion Criteria: \-

Primary outcome measure(s)

  • Incidence of major hemorrhagic and/or thrombotic events — 7 days postoperatively
    Proportion of patients experiencing at least one major hemorrhagic event (BARC grade ≥3, including hemoglobin drop ≥3 g/dL, red blood cell transfusion attributed to bleeding, need for interventional procedure, hemorrhagic shock, or documented intracranial hemorrhage) and/or thrombotic complication (imaging-confirmed ischemic stroke, acute mesenteric ischemia requiring surgery, acute limb ischemia, or vascular thrombosis) within 7 days after surgery.

Trial sites (1)

FacilityCityRegionStatus
Hôpital Universitaire La Pitié-Salpêtrière Paris France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07817680 on ClinicalTrials.gov ↗ ← All trials in France