drugset / Trial / NCT05774691

Routine Versus Selective Protamine Administration to Reduce Bleeding Complications After Transcatheter Aortic Valve Implantation (POPular ACE TAVI)

NCT05774691

RandomizedParallel-groupTriple-blindPrevention

Summary

Heparin reversal by protamine administration after transcatheter aortic valve implantation (TAVI) may reduce bleeding events. However, protamine can also cause life-threatening allergic reactions. High-quality evidence regarding the clinical safety and efficacy of routine protamine administration after TAVI is lacking. The aim of this clinical trial is to determine if routine protamine administration, compared with selective protamine administration, reduces the risk of all-cause mortality or clinically relevant bleeding within 30 days after transcatheter aortic valve implantation.

Timeline

Start
2023-11-01
Primary completion
2026-01-02
Completion
2026-01-02

Drugs

EvaluationDrugModalityDoseRoute
Comparator Protamine Sulfate Unknown

Indications