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Safety and usefulness of Enoxaparin versus unfractionated heparin in patients with ST elevation myocardial infarction

Safety and usefulness of Enoxaparin versus unfractionated heparin in patients with ST elevation myocardial infarction

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138711271695N1
Enrollment
150
Registered
2009-04-25
Start date
2006-06-22
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

Ischaemic heart diseases. Acute myocardial infarction

Interventions

Intervention 1: Streptokinase (1.5 million units intravenously over 1 h) plus unfractionated heparin for a minimum of 48 hours and adjusted to the activated partial thromboplastin time according to th
Treatment - Drugs
Streptokinase (1.5 million units intravenously over 1 h) plus unfractionated heparin for a minimum of 48 hours and adjusted to the activated partial thromboplastin time according to the American Heart
Streptokinase (1.5 million units intravenously over 1 h) plus Enoxaparin was administered as an intravenous bolus (40 mg) and then subcutaneously every 12 hrs (1 mg/kg) with a maximum of 100 mg for th

Sponsors

Tehran University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Age range 18 to 75 years old, onset of symptoms of acute myocardial infarction within 12 hrs before randomization, ST-segment elevation of 0.1 mV or more in two or more limbs leads or at least 0.2 mV in two or more precordial leads. Exclusion Criteria: Contraindications to streptokinase, cardiogenic shock, receiving glycoprotein IIb/IIIa antagonists or oral anticoagulants within the prior days or therapeutic dose of heparin or low molecular-weight heparin within the previous hours, need for anticoagulant therapy and also any other disease that resulted in increasing risk

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
ST-segment resolution. Timepoint: 90 minutes after intervention. Method of measurement: ECG.;Ejection Fraction. Timepoint: during 5-10th day of admission. Method of measurement: Angiography.;Thombolysis in Myocardial Infarction (TIMI) flow grade 3 (patency). Timepoint: during 5-10th day of admission. Method of measurement: Through angiography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Reza Pourbehi

Bushehr University of Medical Sciences and Health Services

m_purbehi@yahoo.com+98 77 1252 4044

Outcome results

None listed

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