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Study identifier: NCT06919562 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

OPtimal stEnt Deployment stRategy oF Contemporary sTents - Registry to Evaluate Percutaneous Coronary Intervention Using Bioresorbable Scaffolds With Thinner-strut Construction and Guidance by intracOronary Imaging to REduce Scaffold Failure

Condition: Coronary Arterial Disease (CAD) · Percutaneous Coronary Intervention (PCI)  ·  Sponsor: Albert Schweitzer Ziekenhuis, Netherlands

PhaseN/A
Planned participants117
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Implantation of a metallic drug-eluting stent (DES) is currently the gold standard in percutaneous coronary intervention (PCI). However, a DES has several limitations on the long-term, such as chronic local inflammation which may lead to in-stent restenosis, absence of physiological coronary vasomotion and vessel caging which makes future coronary artery bypass grafting (CABG) impossible. A bioresorbable scaffold (BRS) is designed to overcome these limitations. The first generation BRS was shown to be clinically inferior to DES due to a slightly higher rate of stent thrombosis. To overcome this problem, several scientific developments have been achieved in the past few years, such as thinner BRS strut construction and improved implantation technique by using PSP (predilatation, sizing, postdilatation) method and intracoronary imaging guidance with optical coherence tomography (OCT) or intravasculair ultrasound (IVUS). A PCI protocol that combines implantation of a second generation thin-strut BRS, mandatory PSP implantation method and mandatory intracoronary imaging-guidance has not yet been investigated. The aim of this study is to investigate feasibility of a new PCI protocol with implantation of the second generation Meres100 thin-strut BRS combined with a protocolized PSP implantation technique guided by intracoronary imaging.

This description comes directly from the study's public registry record.

Talk to the study team

Jin M. Cheng, MD, PhD  ·  +31786541492  ·  j.m.cheng@asz.nl

Always discuss trial participation with your own doctor first.

Locations (1)

Albert Schweitzer ziekenhuisDordrecht, NetherlandsRecruiting

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Source record: clinicaltrials.gov/study/NCT06919562