IRIS-BVS AMI Registry (IRIS BVS AMI)

Duk-Woo Park, MD

Status: Terminated

Conditions: Coronary Artery Disease; Arterial Occlusive Diseases; Cardiovascular Diseases

Treatments: Device: Bioresorbable Vascular Scaffold

Study type: Observational

Funder types: Other

Identifiers

NCT02699671

AMCCV2016-01

Details and patient eligibility

About

The purpose of this study is to evaluate the relative effectiveness and safety of Bioresorbable Vascular Scaffold in acute myocardial infarction compared to other (drug eluting stents) DES.

Enrollment: 69 patients

Sex: All

Ages: 19+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age 19 and more
• Acute myocardial infarction
• Intervention with Bioresorbable Vascular Scaffold
• Agreed with written informed consent form

Exclusion criteria

• Bypass graft surgery (CABG) recommended
• Lesion with previous bypass graft surgery (CABG)
• Severe calcification and/or severe tortuosity
• Contraindication to antiplatelet agent or Inability to take dual antiplatelet therapy within 1 year
• Life expectancy of 1year and under
• Subjects scheduled to receive cardiac surgery or serious non-cardiac surgery
• Cardiac shock

Trial design

69 participants in 1 patient group

acute myocardial infarction

Treatment:

Device: Bioresorbable Vascular Scaffold