Skip to main content
OpenTrials
Completed

NCT Number: NCT04927949

Evaluation of Myocardial Reperfusion After Primary PCI in Patients With High Platelet Reactivity Treated by Cangrelor or Not

This study aims to evaluate the impact on myocardial reperfusion and residual thrombotic burden of adding Cangrelor -a potent and immediate P2Y12 inhibitor- to ticagrelor in primary PCI patients with high on ticagrelor platelet reactivity compared to standard of care with ticagrelor alone.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

CAEN University Hospital

Caen, 14000, France

About this study

Despite the use of potent P2Y12 inhibitor such as ticagrelor, half of the patients presented high platelet reactivity (HPR) at the time of primary percutaneous coronary intervention (PCI) for ST-elevation myocardial infarction (STEMI). HPR has been associated with impaired myocardial reperfusion. Myocardial reperfusion, assessed using myocardial blush grade, is a strong prognostic factor associated with infarct size and mortality. Antiplatelet therapy intensification using a potent and immediate P2Y12 inhibitor such as Cangrelor according a point-of-care platelet function test has not been studied in the acute phase of STEMI.

This study aims to evaluate the impact on myocardial reperfusion and residual thrombotic burden of adding Cangrelor to ticagrelor in primary PCI patients with high on ticagrelor platelet reactivity compared to standard of care with ticagrelor alone.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patient admitted for STEMI within 24 hours from symptom onset
  • pretreated with ticagrelor, aspirin and enoxaparin (according local protocol)
  • successfully treated by primary PCI of a native coronary culprit lesion
  • anatomy accessible to optical coherence tomography (OCT or OFDI)

Exclusion criteria

  • cardiogenic shock
  • stent restenosis or thrombosis
  • use of glycoprotein IIb/IIIa inhibitors before or during PCI
  • known coagulation disease
  • high bleeding risk (thrombocytopenia <100,000/dL, surgery <30 days, active bleeding)
  • uncontrolled arterial hypertension (>180/110 mmHg)
  • history of stroke (ischemic or hemorrhagic) or transient ischemic attack
  • known severe renal insufficiency (eGFR <30 ml/min)
  • oral anticoagulation

Treatment and study plan

cangrelor perfusion during PCI

Drug

Cangrelor perfusion (started before PCI) with intravenous bolus of 30 microgram/kg, followed by a perfusion of 4 microgram/kg/min during 2 hours or until the end of the PCI if longer

standard PCI

Procedure

primary PCI without cangrelor

Primary outcomes

  1. Grade of myocardial blush

    Time frame: during procedure

    myocardial blush grade from 0 to 3 (normal)

Secondary outcomes

  1. percentage of residual thrombus burden

    Time frame: during procedure

    intrastent residual thrombus burden assessed by optical coherence tomography

  2. measure of platelet reactivity

    Time frame: during procedure

    Platelet reactivity using VerifyNow after PCI for patients with basal platelet reaction unit>208

  3. troponin

    Time frame: day 1

    peak value

  4. infarct size and no reflow on MRI

    Time frame: during hospitalization assessed up to 7 days

  5. clinical outcomes

    Time frame: during hospitalization assessed up to 7 days

    death, new myocardial infarction, stent thrombosis, new revascularization, stroke, major bleeding

Sponsors and collaborators

Lead sponsor

University Hospital, Caen

Other

Collaborators

  • Terumo Medical Corporation

Registry information

Official study title

Evaluation of Myocardial Reperfusion and Residual Thrombotic Burden After Primary PCI for STEMI in Patients With High on Ticagrelor Platelet Reactivity Treated by IV Cangrelor Versus Ticagrelor Alone

Acronym: ERMIT

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Jun 16, 2021
Registry last updated
Apr 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.