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A multicenter clinical study on left ventricular myocardial work in predicting the efficacy of cardiac resynchronization therapy

A multicenter clinical study on left ventricular myocardial work in predicting the efficacy of cardiac resynchronization therapy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500115226
Enrollment
Unknown
Registered
2025-12-24
Start date
2025-12-25
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Cardiac Resynchronization

Interventions

Patients with heart failure complicated with LBBB to be treated by CRT:None
LBBB patients with LVEF reservation:None
LVEF reduction in non-LBBB patients:None
Healthy control group:None

Sponsors

The First Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Healthy adults 1) Age >=18 years old; 2) Normal blood pressure (139-90/89-60 MMHG); 3) Body mass Index (BMI) =150ms; LBBB;" The best drug treatment should be at least three months before implantation 2) Age: 18-79 years old 3. LBBB patients with LVEF preservation: LVEF>=53%; LBBB 2) Age: 18-79 years old 4. Non-lbbb patients with reduced LVEF: 1) LVEF<=35%, not LBBB 2) Age: 18-79 years old

Exclusion criteria

Exclusion criteria: 1. Healthy adults 1) Suffering from diseases such as hypertension, diabetes, hyperthyroidism, and arrhythmia; 2) Suffering from connective tissue diseases such as systemic lupus erythematosus, polymyositis, rheumatoid arthritis, etc. 3) Have a history of blood diseases, severe infections or other systemic diseases; 4) Have taken vasodilator drugs within the past month; 5) Peripheral vascular disease, with arterial occlusion where blood flow signals cannot be detected; 6) Those who are unable to cooperate with the examination. 2. Patients with heart failure complicated with LBBB who are scheduled for CRT treatment: 1) Suffering from connective tissue diseases such as systemic lupus erythematosus, polymyositis, and rheumatoid arthritis; 2) Have a history of blood diseases, severe infections or other systemic diseases; 3) Those who are unable to cooperate with the examination. 3. LBBB patients with LVEF preservation: 1) Suffering from connective tissue diseases such as systemic lupus erythematosus, polymyositis, and rheumatoid arthritis; 2) Have a history of blood diseases, severe infections or other systemic diseases; 3) Those who are unable to cooperate with the examination. 4. Non-lbbb patients with reduced LVEF: 1) Suffering from connective tissue diseases such as systemic lupus erythematosus, polymyositis, and rheumatoid arthritis; 2) Have a history of blood diseases, severe infections or other systemic diseases; 3) Those who are unable to cooperate with the examination.

Design outcomes

Primary

MeasureTime frame
Global Work Index;Global Constructive Work;Global Wasted Work;Global Work Efficiency;Left ventricular ejection fraction;Left ventricular end-diastolic diameter;Left ventricular end-systolic diameter;Left ventricular end-diastolic volume;Left ventricular end-systolic volume, stroke volume;

Secondary

MeasureTime frame
Systolic pressure;Diastolic pressure;Ascending aortic diameter;Aortic root diameter;Aortic sinus diameter;Sinotubular junction diameter;Interventricular septal thickness;Left atrial anteroposterior, superior-inferior, and lateral diameters;Right atrial superior-inferior and lateral diameters;Main pulmonary artery diameter;Right ventricular area change rate;Inferior vena cava diameter;

Countries

China

Contacts

Public ContactChunyan Ma

The First Hospital of China Medical University

cmu1h_mcy@126.com+86 24 8328 2129

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026