Coronary Heart Disease Clinical Trial
— EECPVFOfficial title:
A Prospective, Randomized Study of Enhanced External Counterpulsation Therapy on Ventricular Function in Patients With Coronary Heart Disease
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 |
Verified date | October 2020 |
Source | Sun Yat-sen University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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
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 |
Country | Name | City | State |
---|---|---|---|
China | The First Affiliated Hospital, Sun Yat- sen University | Guangzhou | Guangdong |
Lead Sponsor | Collaborator |
---|---|
Sun Yat-sen University |
China,
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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