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EECP Intervention and Coronary Flow Reserve in Chronic Coronary Syndrom : A Multicenter, Randomized Control Study in China

EECP Intervention and Coronary Flow Reserve in Chronic Coronary Syndrom : A Multicenter, Randomized Control Study in China

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079915
Enrollment
Unknown
Registered
2024-01-16
Start date
2023-02-20
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Chronic coronary syndrome

Interventions

EECP treatment group:received a complete ECP course based on the second-stage preventive drug treatment for coronary heart disease

Sponsors

The Eighth Affiliated Hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Able to understand the purpose of the study, voluntarily participate in the study and sign the informed consent; 2) Age =18 years old, gender unlimited; 3) Patients who have received coronary artery CTA examination and visually detected at least one major coronary artery with a diameter of > 2mm and at least one stenosis of 50%-90%, or have previously implanted stents and residual moderate or higher stenosis, and no left main artery lesions; 4) Patients with chronic coronary syndrome who plan to receive further treatment.

Exclusion criteria

Exclusion criteria: 1) Patients after coronary artery bypass grafting; 2) Coronary CTA examination or previous coronary angiography showed =50% of untreated left main lesions; 3) Arrhythmia; 4) Patients after permanent pacemaker or defibrillator implantation; 5) aortic insufficiency, aortic aneurysm, aortic dissection; 6) Coronary artery fistula or severe coronary aneurysm; 7) Symptomatic congestive heart failure or acute myocardial infarction; 8) valvular heart disease, congenital heart disease, cardiomyopathy; 9) Cerebral hemorrhage, bleeding disorder or definite bleeding tendency within 6 months; 10) Warfarin uses international standardized ratio >2.0; 11) Lower extremity infection, phlebitis, varicose veins, deep vein thrombosis; 12) Progressive malignant tumors or diseases with poor prognosis; 13) Uncontrolled hypertension, defined as SBP=180mmHg or DBP=110mmHg; 14) Pregnant women; 15) There are any other factors that the investigator considers inappropriate for inclusion in this study or for the completion of the study.

Design outcomes

Primary

MeasureTime frame
CT Flow reserve fraction;

Secondary

MeasureTime frame
Differences in cardiovascular magnetic resonance imaging;Differences in cardiac ultrasound examination;Differences in cardiopulmonary exercise testing;Differences in continuous non-invasive blood pressure measurement systems;

Countries

China

Contacts

Public ContactGuifu Wu

The Eighth Affiliated Hospital, Sun Yat-sen University

wuguifu@mail.sysu.edu.cn+86 159 8989 3111

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 5, 2026