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A Prospective, Randomized, Blind, Controlled Multicenter Clinical Study Comparing the Effectiveness of Preventive Ventricular Arrhythmia Ablation on the Prognosis After Left Ventricular Assist Device (LVAD) Surgery.

NCT07589738 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2026-05-15

No results posted yet for this study

Summary

To compare the preventive effect of preventive ventricular arrhythmia ablation on the composite events 30 days after surgery in the study population. The composite events defined in this study 30 days after surgery include persistent ventricular tachycardia/ventricular fibrillation, all-cause death, mechanical thrombosis and right heart failure.

Conditions

  • CHF - Congestive Heart Failure

Interventions

PROCEDURE

preventive ablation group

for patients undergoing LVAD surgery while also undergoing prophylactic ablation of ventricular arrhythmias at the same time

Sponsors & Collaborators

  • Shenzhen Core Medical Technology CO.,LTD.

    collaborator INDUSTRY

  • Jiangsu Provincial People's Hospital (The First Affiliated Hospital of Nanjing Medical University)

    collaborator UNKNOWN

  • The First Affiliated Hospital of Bengbu Medical University

    collaborator OTHER

  • Lu'an People's Hospital of Anhui Province

    collaborator UNKNOWN

  • The First Affiliated Hospital of Xuzhou Medical College

    collaborator UNKNOWN

  • First Affiliated Hospital of Wannan Medical College

    collaborator OTHER

  • The First Affiliated Hospital of Anhui Medical University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-01-31
Primary Completion
2028-09-30
Completion
2028-09-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07589738 on ClinicalTrials.gov