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Coronary Bifurcation Lesions clinical trials

View clinical trials related to Coronary Bifurcation Lesions.

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NCT ID: NCT05100992 Recruiting - Clinical trials for Coronary Artery Disease

Progress Bifurcation Global Registry

Start date: April 23, 2020
Phase:
Study type: Observational

Coronary bifurcation lesions are lesions (or blockages) that occur at or near the intersection of a major coronary artery and one of the arteries' side branches. Numerous techniques and devices have been developed to treat coronary bifurcations; however, these types of lesions remain some of the most challenging, both in terms of procedural success and outcome. This study is designed as an observational, multi-center registry that will collect information on treatment strategies and outcomes of consecutive patients undergoing percutaneous coronary interventions (PCI) in coronary bifurcations among various participating centers, in order to determine the frequency of bifurcation PCI, the procedural strategies utilized, and the procedural outcomes.

NCT ID: NCT04899583 Recruiting - Clinical trials for Coronary Bifurcation Lesions

ACOART SCB BIF: Treatment of Coronary Bifurcation Lesion by Sirolimus Coated Balloon vs Paclitaxel Coated Balloon

Start date: November 10, 2021
Phase: N/A
Study type: Interventional

The aim of this randomized controlled trial is to examine the treatment of coronary bifurcation lesion with a sirolimus coated balloon versus a paclitaxel coated balloon. This trial is designed as prospective, multicenter, randomized and open-label.

NCT ID: NCT04896177 Recruiting - Clinical trials for Coronary Bifurcation Lesions

Sirolimus DEB in Coronary Bifurcation Lesions

Start date: March 18, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of sirolimus drug-eluting coronary balloon catheter in treatment of coronary bifurcation lesions. This is a prospective, multicenter, randomized controlled, non-inferior clinical trial, which would enroll 280 participants in total. Paticipants would undergoing PCI with sirolimus DEB or paclitaxel DEB, and be followed-up to 24 months.