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Completed

NCT Number: NCT02298543

Coronary Spasm Presenting Aborted Sudden Cardiac Death, the Multicenter Registry

The purpose of this study is to evaluate the natural course of coronary spasm patients presenting aborted sudden cardiac death and analyze risk factors.

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Key information

Conditions

Coronary Vasospasm Cardiac Death Cardiovascular Diseases Coronary Disease Death Heart Diseases Myocardial Ischemia Pathologic Processes Pathological Conditions, Signs and Symptoms Vascular Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Asan Medical Center

Seoul, Songpa-gu, 138-736, South Korea

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 18 and more
  • Coronary spasm

Exclusion criteria

  • Life expectancy less than 2years
  • Coronary stenosis 50% and more
  • Structural abnormalities of the heart leading to ventricular arrhythmia

Treatment and study plan

coronary spasm

Other

Primary outcomes

  1. all cause death

    Time frame: 1 year

  2. myocardial infarction

    Time frame: 1 year

  3. ventricular tachycardia

    Time frame: 1 year

  4. ventricular Fibrillation

    Time frame: 1 year

Sponsors and collaborators

Lead sponsor

Seung-Jung Park

Other

Registry information

Official study title

The Multicenter Registry to Evaluate the Natural Course of Coronary Spasm Patients Presenting Aborted Sudden Cardiac Death

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Nov 24, 2014
Registry last updated
Dec 30, 2015

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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