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Clinical Trials/NCT03928119
NCT03928119
Unknown
Not Applicable

Construction of Modern reGional Network for Acute Myocardial Infarction

Guangdong Provincial People's Hospital8 sites in 1 country7,102 target enrollmentAugust 1, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Coronary Heart Disease
Sponsor
Guangdong Provincial People's Hospital
Enrollment
7102
Locations
8
Primary Endpoint
Receipt of reperfusion therapy within 12 hoursInfarction patients
Last Updated
3 years ago

Overview

Brief Summary

Incidence of ST-segment Elevation Myocardial Infarction (STEMI) is rising and the existing emergency medical aid system for STEMI was not enough for timely perfusion treatment. No existing research with high-quality data focuses on the characteristic of STEMI incidence and regional network construction. Aiming of Guangdong GAMI(reGional network for Acute Myocardial Infarction) project is to establish effective collaborative regional network system for STEMI patients treatment.

Detailed Description

The project of Guangdong GAMI(reGional network for Acute Myocardial Infarction) is being conducted during 2015-2019 in eight districts with diverse economic development across southern China (Integrated care model was conducted in four regions, which mainly included community public education, non primary-PCI capable centre and referral system improvement, and inhospital green-channal optimization for primary-PCI capable centre. Other four centers were underwent usual care of acute myocardial infacrtion public and medical health service). All the ST-segment elevation myocardial infarction (STEMI) patients admitted in the hospital within 30 days from the symptom onset were enrolled. The key data of the timeline of STEMI onset and treatment were precisely recorded. Other details of STEMI treatment in hospitals such as laboratory data and medication were also collected. During the research period, actions of both optimizing the regional STEMI patients transfer and treatment to shorten the medical delay, as well as educating the public to improve their awareness of early treatment of STEMI were taken meanwhile. In addition, laboratory data, medication, and follow-up information were recorded in a database for further analysis regarding the STEMI patient treatment.

Registry
clinicaltrials.gov
Start Date
August 1, 2015
End Date
February 28, 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jiyan Chen

Professor

Guangdong Provincial People's Hospital

Eligibility Criteria

Inclusion Criteria

  • All adult patients who suspected diagnosis with STEMI.

Exclusion Criteria

  • patients refused to undergo coronary angiography;
  • patients were confirmed as non-STEMI by coronary angiography or the course of STEMI over 1 month;
  • patients occurred onset STEMI during hospitalization in hospitals

Outcomes

Primary Outcomes

Receipt of reperfusion therapy within 12 hoursInfarction patients

Time Frame: From 1 month before hospitalization to 24 hours after hospitalization

The primary outcome was the proportion of patients who received symptom-to-reperfusion treatment within 12 hours.

Secondary Outcomes

  • In-hospital clinical outcomes(30 days)
  • 1-year all-cause mortality(1 year)
  • Onset-to-admission time within 12 hours(From 1 month before hospitalization to 24 hours after hospitalization)
  • Door-to-balloon time within 90 minutes(24 hours)

Study Sites (8)

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