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NCT06924684Active, not recruitingPhase 2

High-Dose Rosuvastatin Preloading for Enhanced Outcomes in STEMI Patients Undergoing Primary PCI

Efficacy Of High-Dose Rosuvastatin Preloading Before Primary Percutaneous Coronary Intervention In Patients Suffering From St-Elevation Myocardial Infarction

Source: ClinicalTrials.gov · Last updated 11 Apr 2025

Brief summary (registry, in English)

To compare the efficacy of high dose rosuvastatin preloading vs placebo before primary PCI in terms of MACE at 30 days

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
66 (estimated)
First submitted
30 Dec 2024
Start date
2 Dec 2024
Primary completion date
23 Jun 2025
Lead sponsor
Sheikh Zayed Federal Postgraduate Medical Institute
NCT number
NCT06924684

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 66
  • From 2 Dec 2024 to the primary completion date, 23 Jun 2025
  • 2 sites 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

  • Hemodynamically unstable patients. History or clinical evidence of any co-morbidities. Taking any medications regularly even statins.

Who the study is looking for

  • Age 18-75 years Patients undergoing primary angiography

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

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

SiteCityCountrySite status
Shaikh Zayed Hsopital
Coordinator of this site? Confirm its status
LahorePakistanUnknown status
Punjab Institute of Cardiology
Coordinator of this site? Confirm its status
LahorePakistanUnknown status

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