Recruiting NA ST Elevation Myocardial Infarction

Compares treatment options for ST Elevation Myocardial Infarction

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)

ClinicalTrials.gov ID: NCT05967663

What this study is testing

What it's testing
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.
  • Which group you join is decided by chance.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 and older

You may be able to join if

  • Age ≥ 18 years
  • Patients presenting STEMI and multivessel coronary disease successful primary PCI of the culprit lesion (including those who still have ischemic...
  • Multivessel disease was defined at least one non-culprit coronary arteries with a diameter of 2.5 mm or more and a maximum diameter at least 50%...
  • Sign an informed consent form before participating in the study

You likely can't join if

  • Received thrombolytic therapy
  • Cardiac shock or SBP\<90mmHg;
  • History of old myocardial infarction;
  • Left main artery lesion, non infarct related vessels are CTO lesions;
  • PCI in the previous 30 days or Previous CABG
  • Patients who cannot give informed consent or have a life expectancy of less than 1 year
See the full eligibility criteria
Who can join
  • Age ≥ 18 years
  • Patients presenting STEMI and multivessel coronary disease successful primary PCI of the culprit lesion (including those who still have ischemic symptoms within 48 hours)
  • Multivessel disease was defined at least one non-culprit coronary arteries with a diameter of 2.5 mm or more and a maximum diameter at least 50% stenosis by visual estimation, PCI can be successfully implemented
  • Sign an informed consent form before participating in the study
What rules you out
  • Received thrombolytic therapy
  • Cardiac shock or SBP\<90mmHg;
  • History of old myocardial infarction;
  • Left main artery lesion, non infarct related vessels are CTO lesions;
  • PCI in the previous 30 days or Previous CABG
  • Patients who cannot give informed consent or have a life expectancy of less than 1 year
  • Patients combined with other serious diseases such as severe renal dysfunction (creatinine clearance value\<30ml/min;), liver dysfunction and thrombocytopenia
  • Patients with severe valve disease, hypertrophic cardiomyopathy, restrictive cardiomyopathy, and primary pulmonary hypertension;
  • Not suitable for clinical research:
  • Currently participating in another study that may affect the primary endpoint
  • Pregnant and lactating women;
  • Known allergy to drugs that may be used in the study;
  • Unable to comply with the trial protocol or follow-up requirements; Or the researcher believes that participating in the trial may result in patients facing greater risks.

The study team makes the final eligibility decision.

Where it's taking place

  • Shanghai, China

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Shanghai, China. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.