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NCT07519590Completed

One-Time Complete Revascularization Versus Staged PCI in MVD During Pharmaco-Invasive STEMI Strategy

One Time Complete Revascularization Versus Staged PCI in Multivessel Coronary Artery Disease During Pharmaco Invasive STEMI Strategy

Source: ClinicalTrials.gov · Last updated 9 Apr 2026

Brief summary (registry, in English)

This study compares two treatment strategies in patients with ST-elevation myocardial infarction (STEMI) and multivessel coronary artery disease (MVD) undergoing a pharmaco-invasive approach after successful fibrinolysis. The study evaluates whether one-time complete revascularization, in which the culprit and significant non-culprit lesions are treated during the same percutaneous coronary intervention (PCI) session, is better than a staged strategy, in which non-culprit lesions are treated in a separate percutaneous coronary intervention (PCI) procedure within 1 month. The hypothesis is that one-time complete revascularization may reduce hospitalization time, cost, and recurrent ischemic symptoms without increasing short-term complications. Participants are adults with acute ST-elevation myocardial infarction (STEMI) and multivessel coronary artery disease (MVD) who had successful fibrinolysis followed by coronary angiography and percutaneous coronary intervention (PCI). Outcomes include total hospitalization time, total expenses, contrast-induced nephropathy (CIN) within 72 hours, and major adverse cardiovascular events (MACE) during 3 months of follow-up.

Status (registry)
Completed
Study type
Interventional
Enrollment
112 (actual)
First submitted
2 Apr 2026
Start date
30 Apr 2023
Primary completion date
30 Jul 2024
Lead sponsor
Tanta University
NCT number
NCT07519590

What you commit to

  • Study type: Interventional
  • Participants enrolled: 112
  • From 30 Apr 2023 to the primary completion date, 30 Jul 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Single-vessel coronary artery disease treated with a pharmaco-invasive strategy.
  • Prior cardiac surgery.

Other illness

  • Stent thrombosis.
  • Severe valvular heart disease.
  • Congenital heart disease.
  • Severe hepatic impairment.
  • Severe renal impairment.

Other

  • Primary percutaneous coronary intervention.
  • Unsuccessful fibrinolysis requiring rescue percutaneous coronary intervention.
  • Candidacy for coronary artery bypass grafting after angiography.
  • Failed complete revascularization.
  • Cardiogenic shock.
  • Chronic total occlusion.
  • Planned percutaneous transluminal coronary angioplasty to a non-culprit lesion in a vessel smaller than 2.5 millimeters with more than 70 percent stenosis.
  • Pregnancy.

Who the study is looking for

  • Adults older than 18 years.
  • Acute ST-elevation myocardial infarction treated with a pharmaco-invasive strategy.
  • Successful fibrinolysis followed by coronary angiography and percutaneous coronary intervention.
  • Multivessel coronary artery disease.
  • Ability to provide written informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Helwan University Hospital
Coordinator of this site? Confirm its status
CairoEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.