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Study identifier: NCT06061627 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Randomized Controlled Trial of LOT-CRT Versus conventionaL BiVP in Heart Failure Patients With NICD

Condition: Heart Failure · Intraventricular Block  ·  Sponsor: The First Affiliated Hospital with Nanjing Medical University

PhaseNA
Planned participants86
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

BATTLE study has been designed as a prospective, multi-center, randomized, controlled trial. This study will enroll 83 patients with chronic heart failure accompanied by intraventricular block (NICD) over an estimated recruitment period of 3 years. An LOT-CRT group will be compared with a group of conventional BiVP in the follow-up of at least 6 months. The study aimed to compare the curative effect of LOT-CRT in preserving LV systolic function with traditional BiVP in chronic heart failure patients with NICD.

This description comes directly from the study's public registry record.

Talk to the study team

Jiangang Zou  ·  86-13605191407  ·  jgzou@njmu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

The First Affiliated Hospital with Nanjing Medical UniversityNanjing, Jiangsu, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06061627