Skip to content

The outcomes of immediate and deferred stenting in primary angioplasty

Comparison of Outcomes following Deferred Versus Immediate Stenting in Patient with ST Elevation Myocardial Infarction Admitted to Emergency Department of Heshmat Hospital at 2015 - 2016

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015120125327N1
Enrollment
57
Registered
2016-01-10
Start date
2016-03-20
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. myocardial infarction specified as acute or with a stated duration of 4 weeks (28 days) or less from onset

Interventions

Intervention 1: Stenting immediately after treatment with aspirin 300 mg and clopidogrel 600 mg heparin 5000 U. Intervention 2: Deferred Group: stenting at least 12 to 168 hours after the primary trea
Treatment - Surgery
Stenting immediately after treatment with aspirin 300 mg and clopidogrel 600 mg heparin 5000 U
Deferred Group: stenting at least 12 to 168 hours after the primary treatment

Sponsors

Vice chancellor for research Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: the duration of symptoms more than six hours, anomalies of involved coronary artery including blocked artery in primary angiography primary perfusion (TIMI0.1) , high volume of thrombosis, high length of lesion (more than 24 mm , small diameter of vessels (less than 5.2 mm ) , clinical signs of acute injury of micro-vascular after primary perfusion (with increasing ST more than 50%) Exclusion criteria include the lack of normal coronary flow (TIMI3) after primary perfusion treatment with thrombus aspiration with or without balloon angioplasty, cardiogenic shock and inability to obtain informed consent.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
No/slow reflow. Timepoint: In the first group (immediate) measured immediately after angiography. Method of measurement: By Echocardiography.This outcome has three degrees : lack of blood flow (TIMI0), incomplete filling (TIMI1), establish low blood flow but with complete filling (TIMI2) in involved coronary artery during or at the end of PCI.

Secondary

MeasureTime frame
The consequences of electrocardiographic. Timepoint: One hour after treatment compared _ basic ECG, before reperfusion. Method of measurement: By electrocardiogram Complete resolution of ST elevation 70% 30 %.;The consequences of Angiographic. Timepoint: At the end of the first procedure as prospective. Method of measurement: By Angiography, stent dimensions are compared with real stent at the second procedure by the same operator.;The consequences of Echocardiography. Timepoint: Before the first procedure and discharge. Method of measurement: Based on wall motion score index.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNozar Sotoudeh Foumani

Guilan University of Medical Sciences

sepehrsaghari67@gmail.com+98 911 933 0305

Outcome results

None listed

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