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Active Not RecruitingNCT06924684

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

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
66 (estimated)
Sponsor
Sheikh Zayed Federal Postgraduate Medical Institute · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

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

Conditions

Interventions

TypeNameDescription
DRUGStatin monotherapy (rosuvastatin or atorvastatin)Tab Rosuvastatin 40mg (weight) at presentation. Tab Rosuvastatin 20mg at night for 30 days.
DRUGPlaceboPlacebo caspule

Timeline

Start date
2024-12-02
Primary completion
2025-06-23
Completion
2025-07-02
First posted
2025-04-11
Last updated
2025-04-11

Locations

2 sites across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT06924684. Inclusion in this directory is not an endorsement.

High-Dose Rosuvastatin Preloading for Enhanced Outcomes in STEMI Patients Undergoing Primary PCI (NCT06924684) · Clinical Trials Directory