Skip to content

Atorvastatin and Rosuvastatin in myocardial infarction

Comparing the effect of preprocedural loading dose of Arorvastatin vs Rrosuvastatin on prevalence of no-reflow and low TIMI flow in patients with ST elevation myocardial infarction undergoing primary percutaneous intervention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200722048166N1
Enrollment
160
Registered
2021-09-10
Start date
2021-08-02
Completion date
Unknown
Last updated
2021-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

acute myocardial infarction. ST elevation (STEMI) and non-ST elevation (NSTEMI) myocardial infarction

Interventions

Intervention 1: Control group: Patients in this group will be treated Atorostatin 80 mg, the first dose will be prescribed in the emergency department and the other doses will be continuous. Interven

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: All patients who are candidates primary percutaneous intervention with acute myocardial infarction with ST-segment elevation are admitted to the emergency department of Madani heart center of Tabriz.

Exclusion criteria

Exclusion criteria: The patients with chronic disease such as inflammatory diseases, renal failure, a history of collagen and vascular disease, current active infection, blood diseases. The patients with history of acute myocardial infarction or ischemic heart disease. The patients with history of diabetes.

Design outcomes

Primary

MeasureTime frame
Rate of no-reflow at the during of PPCI. Timepoint: once at the during of the PPCI. Method of measurement: observational and based on individual skills.;Rate of TIMI flow at the end of PPCI. Timepoint: once at the end of the PPCI. Method of measurement: observational and based on individual skills.

Secondary

MeasureTime frame
Rate of mortality. Timepoint: During hospitalization. Method of measurement: Observational.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNaser Khalili

Tabriz University of Medical Sciences

dr_nkhalili@yahoo.com+98 41 3387 7616

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026