Skip to content

Review of angioplasty of coronary artery on treating patients with myocardial infarction

The Integrilin effect evaluation on the P-PCI on mortality and echocardiography in patients suffered from acute MI and the comparison with P-PCI

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201203139284N1
Enrollment
120
Registered
2012-10-08
Start date
2012-01-21
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

cardiac attack. Acute myocardial infarction

Interventions

Intervention 1: A group treated with integtilin performed immediately before angioplasty. Dose of 180 micrograms per kg body weight integriln unit dosage form is administered before angioplasty follow
Treatment - Drugs
A group treated with integtilin performed immediately before angioplasty. Dose of 180 micrograms per kg body weight integriln unit dosage form is administered before angioplasty followed by a second 1
Group B treated with coronary angioplasty are useful to the common method

Sponsors

Vice chancellor for research, Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Included all patients who present with typical chest pain and their ECG have ST-Elevation changes (less than 6 hours of onset of symptoms, patients should be referred to the emergency room). If patient is admitted between 6 to 12 hours from onset of symptoms and still have chest pain with the st-elevation changes in EKG ,are said to be in the study 2. patients do not have integrilin drug contraindications. Exclusion criteria: 1. patients with Coagulopathic bleeding disorders 2. delay time of 12 hours of pain onset to admission. 3. active bleeding 4. in group A: active bleeding, recent major surgery within 6 weeks, platelet count less than 100000, severe hypertension (> 200/110 mm/Hg), history of stroke or hemorrhagic stroke within 30 days, renal failure

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Ejection fraction. Timepoint: One month later. Method of measurement: Echocardiography.;EKG changes. Timepoint: one month later. Method of measurement: EKG.;Ejection fraction. Timepoint: three months later. Method of measurement: Echocardiography.;EKG changes. Timepoint: three months later. Method of measurement: EKG.

Secondary

MeasureTime frame
Mortality. Timepoint: one month and three months latar. Method of measurement: Total death toll.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBehfar Pakbaz

Arak University of Medical Science

behfar.pakbaz@yahoo.com+98 86 1417 3601

Outcome results

None listed

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