Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05967663

Fractional Flow Reserve Guided Immediate Versus Staged Complete Myocardial Revascularization in Patients With ST-segment Elevation Myocardial Infarction With Multivessel Disease (Future Study)

Led by RenJi Hospital · Updated on 2023-12-04

840

Participants Needed

1

Research Sites

263 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

It is a prospective, multicenter, randomised controlled, open-label, blinded endpoint assessment trial, to compare the strategy of immediate complete revascularisation and staged complete revascularisation in ST-segment-elevation myocardial infarction patients with multivessel coronary disease.

CONDITIONS

Official Title

Fractional Flow Reserve Guided Immediate Versus Staged Complete Myocardial Revascularization in Patients With ST-segment Elevation Myocardial Infarction With Multivessel Disease (Future Study)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Presenting with STEMI and multivessel coronary disease with successful primary PCI of the culprit lesion
  • Multivessel disease defined as at least one non-culprit artery with diameter 2.5 mm or more and at least 50% blockage by visual estimation
  • Ability to sign informed consent before participating in the study
Not Eligible

You will not qualify if you...

  • Received thrombolytic therapy
  • Cardiac shock or systolic blood pressure less than 90 mmHg
  • History of old myocardial infarction
  • Left main artery lesion or chronic total occlusion lesions in non-infarct related vessels
  • PCI in the previous 30 days or previous coronary artery bypass grafting
  • Unable to give informed consent or life expectancy less than 1 year
  • Severe renal dysfunction with creatinine clearance less than 30 ml/min, liver dysfunction, or thrombocytopenia
  • Severe valve disease, hypertrophic cardiomyopathy, restrictive cardiomyopathy, or primary pulmonary hypertension
  • Currently participating in another study that may affect the primary endpoint
  • Pregnant or breastfeeding women
  • Known allergy to drugs used in the study
  • Unable to comply with trial protocol or follow-up requirements or if participation may result in greater risks

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Renji Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

Shanghai, China

Actively Recruiting

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Research Team

J

Jun Pu, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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