Phase
Condition
Heart Failure
Chest Pain
Hyponatremia
Treatment
BiVP group
LOT-CRT group
Clinical Study ID
Ages 18-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Ischemic or non ischemic cardiomyopathy
Optimal medical therapy for at lest 3 months
NYHA class II-IV
LVEF≤35% as assessed by echocardiography
Sinus rhythm (may have paroxysmal atrial fibrillation)
QRS duration ≥ 150ms
Intraventricular block (NICD), QRS morphology is neither LBBB nor RBBB
Exclusion
Exclusion Criteria:
Valvular heart disease that requires or has undergone surgical intervention
After mechanical tricuspid valve replacement
Persistent or permanent atrial fibrillation or atrial flutter
Second or third degree atrioventricular block
Have a history of acute myocardial infarction within 3 months prior to enrollment
Patient's expected survival time is less than 12 months
Pregnant or planned to conceive
Ventricular septal hypertrophy (ventricular septal thickness exceeds 15mm at the endof diastole)
Patients with simple and persistent left superior vena cava
Patients with existing pacemaker implantation
Study Design
Study Description
Connect with a study center
The First Affiliated Hospital with Nanjing Medical University
Nanjing, Jiangsu 210029
ChinaActive - Recruiting

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