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Clinical Study on the Efficacy and Safety of Noninvasive Cardiac Function Monitoring-Guided Individualized Enhanced External Counterpulsation Therapy in Elderly Cardiac Rehabilitation Patients

Clinical Study on the Efficacy and Safety of Noninvasive Cardiac Function Monitoring-Guided Individualized Enhanced External Counterpulsation Therapy in Elderly Cardiac Rehabilitation Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123857
Enrollment
Unknown
Registered
2026-04-30
Start date
2026-03-18
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Cardiovascular Diseases in the Elderly

Interventions

Control (Standard EECP ):The Chongqing Pushikang Technology P-ECP/TI-S pneumatic external counterpulsation device was utilized. The initial cuff pressure was set at 0.018-0.045 MPa by an experienced t
Experimental (NHM-EECP ):Prior to each EECP session, patients were connected to a noninvasive hemodynamic monitor (employing a thoracic electrical bioimpedance-based device from OSYPKA, Germany). Foll
(b) Real-time cardiac index (CI) increased by =10% compared to the pre-treatment resting baseline value
(c) Absence of significant patient discomfort such as dizziness or chest pain. During therapy, real-time monitoring was performed. An automatic alarm would be triggered and the pressure would be reduc

Sponsors

The First Affiliated Hospital of Air Force Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
80 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age = 80 years; 2. Patients with stable coronary artery disease accompanied by one of the following conditions: angina pectoris, chronic heart failure, status post percutaneous coronary intervention (PCI), or old myocardial infarction with evidence of myocardial ischemia; 3.Meeting the indications for Enhanced External Counterpulsation (EECP) therapy and having no contraindications; 4. Having provided written informed consent.

Exclusion criteria

Exclusion criteria: 1. Presence of absolute contraindications to Enhanced External Counterpulsation (EECP), including but not limited to: severe aortic valve insufficiency, active thrombophlebitis, deep vein thrombosis (DVT) of the lower extremities, severe aortic aneurysm, uncontrolled hypertension (blood pressure > 180/110 mmHg); 2. Presence of severe cardiac arrhythmias; 3. Limb deformities or severe peripheral arterial disease that would interfere with proper cuff application of the EECP device; 4.Cognitive impairment precluding cooperation with the assessment/treatment.

Design outcomes

Primary

MeasureTime frame
Cardiac Index (CI);

Secondary

MeasureTime frame
Left Ventricular Ejection Fraction (LVEF);Left Ventricular End-Diastolic Diameter (LVEDD);Left Ventricular End-Systolic Diameter (LVESD);6-Minute Walk Distance (6MWD);NYHA class;CCS class;Quality of sleep; Emotional state;Quality of life;Stroke volume;Cardiac output;Systemic Vascular Resistance;N-terminal pro-B-type natriuretic peptide( NT-proBNP);

Countries

China

Contacts

Public ContactYingjun Gong

The First Affiliated Hospital of Air Force Medical University

gyjkfzls@126.com+86 188 9206 8066

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026