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effect of eptifibatide and reteplase on primary angioplasty outcomes

Comparison of the efficacy of intracoronary and intravenous Eptifibatide and intracoronary Retaplase in thrombus aspiration in patients undergoing Primary percutaneous coronary interventions (PPCI); Randomized clinical trial study)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170925036401N2
Enrollment
160
Registered
2017-12-22
Start date
2017-11-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Acute Myocardial Infarction. Acute myocardial infarction

Interventions

Treatment - Drugs
All patients will receive Emergency PCI treatment. Patients will receive 300 mg of chewing aspirin and 600 mg of Clopidogrel maintenance dose prior to the procedure before transferring to the catheter

Sponsors

Deputy of Research of Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Ischemic typical chest pain extending more than 30 min; ST elevation more than 1 mm in at least 2 leads with the same name; all patients with STEMI candidate for primary PCI; myocardial infarction not extending more than 12 hours; having life expectancy not less than 6 months; consent for participation in the study; age 18 to 80 years; no evidence for prior myocardial infarction; not having contraindications for reteplase or eptifibatide; not having left bundle branch block; not using GPIIb/IIIa in recent two weeks.

Exclusion criteria

Exclusion criteria: Exclusion criteria: Rescue PCI after thrombolytic therapy; emergency CABG; AF; cardiogenic shock; TIMI flow grade 3 in primary angiography

Design outcomes

Primary

MeasureTime frame
Coronary blood flow. Timepoint: before and after primary PCI. Method of measurement: based on angiographic scale TIMI blush grade.

Secondary

MeasureTime frame
Left ventricular diastolic dysfunction change. Timepoint: before and after angiography. Method of measurement: according to echocardiographic criteria.;ST resolution average. Timepoint: before and 90 minutes after PCI. Method of measurement: based on electrocardiogram.;Average of EF changes. Timepoint: before and 3 to 4 days after angioplasty. Method of measurement: based on echocardiography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMostafa Zadkamali

Guilan University of medical sciences

mzadkamali@gums.ac.ir/mhoseinie@yahoo.com/m_zadkamali@yahoo.com+98 13 3366 9064

Outcome results

None listed

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