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Completed

NCT Number: NCT02804958

Incheon-Bucheon Cohort of Patients Undergoing Primary PCI for Acute STEMI

INcheon-Bucheon cohorT of patients undERgoing primary percutaneous coronary intervention for acute ST-ELevation myocardiaL infARction (INTERSTELLAR) registry is a retrospective, observational, 4-regional-hospital based registry reflecting current practices of management, risk factors, and clinical outcomes in patients with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention at cities of Incheon and Bucheon located in the mid-western part of the Korean peninsula between 2007 and 2014.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Sejong General Hospital, Bucheon-si, South Korea

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About this study

INcheon-Bucheon cohorT of patients undERgoing primary percutaneous coronary intervention for acute ST-ELevation myocardiaL infARction (INTERSTELLAR) registry is a retrospective, observational, 4-regional-hospital based registry reflecting current practices of management, risk factors, and clinical outcomes in patients with ST-segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PCI) at cities of Incheon and Bucheon located in the mid-western part of the Korean peninsula between 2007 and 2014. Diagnosis of acute STEMI was based on clinical data findings including typical symptoms, 12-lead electrocardiography, and blood test. Decisions regarding primary PCI were made by at least 2 attending cardiologists at the time of presentation.

Demographic data, cardiovascular risk factors, laboratory data and clinical follow-up data were collected. Baseline blood test was obtained and recorded as part of the routine care for patients who visited the emergency room for chest pain and in whom acute coronary syndrome was suspected. Standard medical management was provided by responsible physicians.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients diagnosed with acute ST-segment elevation myocardial infarction
  • Patients treated with primary percutaneous coronary intervention

Exclusion criteria

  • Patients diagnosed with Non-ST-segment elevation acute coronary syndrome
  • Patients treated with thrombolytic therapy

Treatment and study plan

STEMI treated with primary PCI

Procedure

Primary percutaneous coronary intervention was performed according to the current standard guidelines. Coronary angiography was performed using standard techniques. The use of thrombectomy devices, intravascular ultrasound, intra-aortic balloon pump, and percutaneous cardiopulmonary support was up to the operator.

Primary outcomes

  1. MACCE

    Time frame: Within the 1 year

    Major adverse cardiac and cerebrovascular event (MACCE), defined as the composite of all-cause death, non-fatal myocardial infarction and non-fatal stroke

Secondary outcomes

  1. All-cause death

    Time frame: Within the 1 year

  2. Non-fatal myocardial infarction

    Time frame: Within the 1 year

  3. Non-fatal stroke

    Time frame: Within the 1 year

  4. Ischemic-driven revascularization

    Time frame: Within the 1 year

  5. Admission for heart failure

    Time frame: Within the 1 year

Sponsors and collaborators

Lead sponsor

Gachon University Gil Medical Center

Other

Collaborators

  • Inha University Hospital
  • Sejong General Hospital
  • Soon Chun Hyang University

Registry information

Official study title

Incheon-Bucheon Cohort of Patients Undergoing Primary Percutaneous Coronary Intervention for Acute ST-segment Elevation Myocardial Infarction

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Jun 17, 2016
Registry last updated
Jun 17, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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