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Effect of Code STEMI on "Door to balloon time"

The effect of activation and implementation of the Code STEMI on "Door to balloon time" in patients with myocardial infarction with ST-segment elevation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171210037814N1
Enrollment
50
Registered
2018-03-13
Start date
2017-11-22
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

Acute myocardial infarction.

Interventions

Intervention 1: Control group: The control group is a patient who has been diagnosed with acute myocardial infarction with ST segment elevation before applying the "STEMI code". and transferring them

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients with acute and typical heart disease referred to the emergency department of the selected treatment center affiliated with Qazvin University of Medical Sciences. Patients should be referred by EMS. The diagnosis of acute STEMI in patients should be confirmed by a cardiologist.

Exclusion criteria

Exclusion criteria: Referral of the patient to the hospital after more than 12 hours from the onset of pain. Referral of patient from other treatment centers. Patients hospitalized in other parts of the hospital who have had a new heart attack. Not satisfying the patient for primary angioplasty.

Design outcomes

Primary

MeasureTime frame
"Door to balloon" time. Timepoint: Before and after applying "STEMI code". Method of measurement: Time recording.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJalalian Fateme

Qazvin University of Medical Sciences

f54.jalalian@gmail.com+98 28 3336 6428

Outcome results

None listed

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