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Clinical Trials/NCT06503640
NCT06503640
Recruiting
N/A

Coronary Microvascular Dysfunction in Angina Patients With Non-obstructive Coronary Artery Disease

China-Japan Friendship Hospital1 site in 1 country100 target enrollmentJuly 1, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Angina Patients With Non-obstructive Coronary Artery Disease
Sponsor
China-Japan Friendship Hospital
Enrollment
100
Locations
1
Primary Endpoint
MACE in 12 months
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The goal of this observational study is to explore the incidence and effect on prognosis of coronary microvascular dysfunction in patients present of stable anginal symptoms, a clinical indication for invasive coronary angiography, and no hemodynamically significant epicardial coronary artery disease, defined as fractional flow reserve (FFR) >0.80.

Registry
clinicaltrials.gov
Start Date
July 1, 2023
End Date
December 31, 2025
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
China-Japan Friendship Hospital
Responsible Party
Principal Investigator
Principal Investigator

Jingang Zheng

Head of Cardiology Department

China-Japan Friendship Hospital

Eligibility Criteria

Inclusion Criteria

  • presence of stable anginal symptoms, a clinical indication for invasive coronary angiography, and no hemodynamically significant epicardial coronary artery disease, defined as fractional flow reserve (FFR) \>0.80

Exclusion Criteria

  • acute myocardial infarction
  • significant valvular heart disease
  • advanced chronic kidney disease
  • patients with significant epicardial coronary artery stenosis (\>70% in major vessels by diagnostic coronary angiography) needing percutaneous coronary intervention
  • patients unable to provide written informed consent

Outcomes

Primary Outcomes

MACE in 12 months

Time Frame: 12 months

major adverse cardiovascular events 12 months, including cardiac death, myocardial infarction, and readmission for angina.

Study Sites (1)

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