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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03106116
Other study ID # EECP-3
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 15, 2017
Est. completion date March 30, 2019

Study information

Verified date October 2020
Source Sun Yat-sen University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the efficacy of Enhanced External Counterpulsation (EECP) therapy on ventricular function in patients with coronary heart disease


Description:

Patients with coronary heart disease will be randomized into two groups: standard medical treatment and standard medical treatment plus EECP intervention. Ventricular structure and function will be measured and compared.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date March 30, 2019
Est. primary completion date December 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - More than 50% stenosis of left main trunk and 3 epicardial coronary arteries and their large branches showed by coronary angiography - Or history of myocardial infarction - Or history of prior revascularization - Signed informed consent to participate in the study Exclusion Criteria: - Clinically significant valvular heart disease - Aortic aneurysm - Congenital heart disease - Acute myocarditis - Arrhythmias significantly interfere with the triggering of the EECP device - History of cerebral hemorrhage - Hemorrhagic disease - Lower limb infection, phlebitis - Deep venous thrombosis - Malignant disease - International normalized ratio (INR) > 2.5 - Uncontrolled hypertension, defined as systolic blood pressure > 180mmHg or diastolic blood pressure > 110mmHg - Pregnancy

Study Design


Intervention

Device:
Experimental: Enhanced External Counterpulsation
Enhanced External Counterpulsation (EECP) is a technique for assisting the circulation by decreasing the afterload of the left ventricle and augmenting the diastolic pressure externally by applying a negative pressure to the lower extremities during cardiac systole. EECP therapy has been approved by the United States Food and Drug Administration (FDA) for the treatment of refractory angina and heart failure. Administration of 35-36 hours EECP therapy over a 7 week period, one hour session every working day.
Drug:
Standard medical therapy
Guideline- driven standard medical treatment for 7 weeks

Locations

Country Name City State
China The First Affiliated Hospital, Sun Yat- sen University Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Sun Yat-sen University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in heart function Change from baseline in heart function assessed by trans- thoracic echocardiography at 7 weeks 7 weeks
Secondary Change in cardiac chamber diameter Change from baseline in cardiac chamber diameterat 7 weeks 7 weeks
Secondary Change in ventricular wall thickness Change from baseline in ventricular wall thickness 7 weeks
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