Efficacy of Enhanced External Counterpulsation on Ventricular Function
NCT03106116 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150
Last updated 2020-11-02
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
Conditions
Interventions
- 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
Sponsors & Collaborators
-
Sun Yat-sen University
lead OTHER
Principal Investigators
-
Yan Zhang, M. D. · First Affiliated Hospital, Sun Yat-Sen University
-
Zhensheng Zheng, M. D. · First Affiliated Hospital, Sun Yat-Sen University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 90 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-03-15
- Primary Completion
- 2018-12-30
- Completion
- 2019-03-30
Countries
- China
Study Locations
More Related Trials
-
Use of Artificial Intelligence Cardiac Ultrasound Technology in Teaching Point of Care Cardiac Ultrasound
NCT05297877 ·Status: UNKNOWN ·Phase: NA
-
Comparative Study to Examine Whether Echocardiography Performed During Cardiac Resynchronization Therapy Device Implantation Can Improve the Response Rate
NCT01014000 ·Status: WITHDRAWN ·Phase: NA
-
Multi Point Pacing vs. Conventional STUDY PROTOCOL
NCT04334018 ·Status: WITHDRAWN ·Phase: NA
-
3D Echocardiographic Assessment of Epicardial Pacing After Cardiopulmonary Bypass.
NCT02842762 ·Status: UNKNOWN ·Phase: NA
-
EXecution of Trans-Esophagus Echo Cardiogram in CardioPulmonary Resuscitation for Patients With Out-of-hospital Cardiac Arrest
NCT05907460 ·Status: COMPLETED ·Phase: NA
-
Echocardiography and Peak Endocardial Acceleration (PEA) Measurements in Cardiac Resynchronization Therapy (CRT)
NCT01066078 ·Status: COMPLETED
-
The Diagnosis and Treatment System of Transesophageal Echocardiography in ICU
NCT03811730 ·Status: UNKNOWN ·Phase: NA
-
Impact of Intraventricular Electrical Activation in Resynchronization Therapy
NCT01270646 ·Status: COMPLETED ·Phase: PHASE2
-
Comparison of Cardiac Resynchronisation Therapy (CRT) Response Using High Frequency (HF) - ECG or Q-LV Guided Optimisation for Left Ventricular, Pacing Site.
NCT05829876 ·Status: RECRUITING ·Phase: NA
-
Magnetocardiography (MCG) Parameters in the Prediction of Future ICD Therapy
NCT04352816 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Early Feasibility Study to Assess Safety and Device Performance of AcoustiCare™
NCT03751904 ·Status: WITHDRAWN ·Phase: NA
-
Development of Novel Physiological CMR Methods in Health and Disease
NCT03854071 ·Status: RECRUITING ·Phase: NA
-
Percutaneous Endocardial Septal Radiofrequency Ablation in Obstructive Hypertrophic Cardiomyopathy
NCT06224621 ·Status: RECRUITING ·Phase: NA
-
Guided Placement of CRT-Leads
NCT00764075 ·Status: COMPLETED ·Phase: NA
-
Assessment of Hearts Deemed Unsuitable for Transplant With the Aim of Expanding the Donor Heart Pool.
NCT01780597 ·Status: UNKNOWN
-
Non-Invasive Cardiac Output Measurement for CRT Optimization
NCT02126241 ·Status: COMPLETED ·Phase: NA
-
Retrospective Cohort Study on Post Analysis on the Link Between the Clinical Heart Rate and Outcomes During PCI
NCT02351674 ·Status: UNKNOWN
-
Prospective, Multicenter, Randomized Controlled, Non-inferior Clinical Study to Evaluate the Safety and Efficacy of Radiofrequency Transseptal Puncture System in Atrial Septul
NCT06990230 ·Status: COMPLETED ·Phase: NA
-
A Phase 1 Feasbility Study Of Volume Intracardiac Echo In Assessment Of Patients With Structural And Valvular Heart Disease Undergoing Percutaneous Transcatheter Therapy
NCT01669551 ·Status: COMPLETED
-
Prevalence and Prognostic Relevance of Tricuspid Regurgitation in Different Heart Failure Entities
NCT04570098 ·Status: COMPLETED
-
Sensor-equipped Ultrathin Pressure Microcatheter Versus Pressure Wire for Physiological Measurements
NCT05417763 ·Status: COMPLETED
-
Assessment of the Force Frequency Relationship of the Myocardium After On-pump CABG Surgery
NCT02407574 ·Status: UNKNOWN ·Phase: NA
-
Prospective Longitudinal Evaluation of AI-ECG in a NEwly Diagnosed Heart Failure
NCT05817136 ·Status: UNKNOWN
-
Comparison of Carotid Peak Systolic Velocity Variation With Aortic Peak Systolic Velocity Variation in Pediatric Non-Cardiac Surgery
NCT03155555 ·Status: COMPLETED
-
Focused Assessed Echocardiography to Predict Fluid Responsiveness
NCT03044405 ·Status: COMPLETED ·Phase: NA