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
Sponsors and collaborators
BrosMed Medical Co., Ltd
Lead sponsor
LanZhou University
Collaborator