Efficacy and Safety of Sirolimus-coated Coronary Balloon Dilatation Catheter for De Novo Coronary Bifurcation Lesions

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorBrosMed Medical Co., Ltd

About this trial

Evaluating the Safety and Efficacy of Sirolimus-coated Coronary Balloon Dilatation Catheter vs Paclitaxel-coated balloon catheter for the Treatment of De Novo Coronary Bifurcation Lesions

Eligibility criteria

Qualifiers

Age ≥18 years and ≤80 years.

Evidence of asymptomatic myocardial ischemia, or stable/unstable angina, or myocardial infarction that occurred more than 7 days before enrollment and is now stable.

Suitable for any type of coronary artery revascularization, such as balloon angioplasty, stent implantation, and coronary artery bypass grafting (CABG).

Capable of understanding the purpose of the trial, willing to participate, and acknowledging the risks and benefits described in the informed consent document by signing the informed consent form, and willing to undergo invasive imaging follow-up.

Disqualifiers

Unstable Arrhythmias: Such as high-risk ventricular premature beats or ventricular tachycardia.

Severe Heart Failure (New York Heart Association Functional Classification, NYHA Class IV).

Preoperative Renal Impairment: Or currently undergoing hemodialysis treatment.

Bleeding Tendencies or Contraindications to Antiplatelet Agents and Anticoagulants: Participants who cannot undergo antithrombotic therapy.

Trial design

Treatments tested in this trial

  • Sirolimus-coated Balloon Dilatation Catheter
  • Paclitaxel-coated Balloon Dilatation Catheter

Treatment groups

250 Participants
are divided into 2 treatment groups

Sponsors and collaborators

BrosMed Medical Co., Ltd

Lead sponsor

LanZhou University

Collaborator