← Eichor
Study identifier: NCT07582835 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study of the Long-term Effects of P2Y12 Inhibitor Monotherapy and Coagulation Markers After Percutaneous Coronary Angioplasty.

Condition: Coronary Artery Disease · Percutaneous Coronary Intervention · Acute Coronary Syndromes  ·  Sponsor: Cardiocentro Ticino

PhasePhase 3
Planned participants355
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Patients who undergo percutaneous coronary intervention (PCI) are commonly treated with antiplatelet therapy to prevent stent thrombosis and recurrence of events. After an initial period of dual antiplatelet therapy, long-term treatment with a single P2Y12 inhibitor (such as clopidogrel, ticagrelor, or prasugrel) is often prescribed. However, the optimal drug and dose for long-term monotherapy remain uncertain, as patients may experience either insufficient platelet inhibition (leading to ischemic events) or excessive inhibition (increasing bleeding risk). The HI-TECH 2 study aims to identify the most appropriate type and dose of P2Y12 inhibitor monotherapy to achieve a balanced level of platelet inhibition within a predefined therapeutic range. The study also seeks to better understand how blood coagulation activity evolves over time after PCI. This is a prospective, investigator-initiated, single-center, open-label study conducted in two phases. In Phase 1, patients receive stepwise reduced doses of ticagrelor or prasugrel to determine the optimal dose that most consistently achieves the desired level of platelet inhibition. In Phase 2, patients are randomly assigned to receive clopidogrel or the optimal doses of ticagrelor or prasugrel identified in Phase 1. The main question of the study is whether optimized ticagrelor or prasugrel regimens are more effective than standard-dose clopidogrel in achieving platelet inhibition within the target therapeutic window, as measur…

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

Talk to the study team

Marco Valgimigli, Cardiology Chief Prof. Dr. Med  ·  +41 (0) 91 811 51 11  ·  marco.valgimigli@eoc.ch

Enrico Frigoli, Dr. Med  ·  +41 (0)91 811 53 04  ·  enrico.frigoli@eoc.ch

Always discuss trial participation with your own doctor first.

Locations (1)

Istituto Cardiocentro TicinoLugano, Ch/ti, SwitzerlandRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07582835