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Clinical Trial Summary

The research aims to compare the response of Cardiac Resynchronisation Therapy (CRT) using HF ECG guided or the conventional method of Q-LV measurement guided optimisation for left ventricular, pacing site.


Clinical Trial Description

The study aims to demonstrate that left ventricular (LV) pacing site optimisation using high frequency (HF) ECG improves LV reverse remodeling response to Cardiac Resynchronization Therapy (CRT), compared with Q-LV (Q-wave on the surface ECG to LV Electrogram) measurement after 6 months of treatment. Participants will be implanted with a Cardiac Resynchronisation Therapy device with either pacemaker or defibrillator function. The study is a single-Centre, randomized, prospective trial. One hundred and eighty participants will be assigned to either the treatment (HF-ECG guided LV pacing site optimisation) or control (Q-LV guided LV pacing site optimisation) arm, employing a 1:1 randomization. The participants will be followed up for a period of 6 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05829876
Study type Interventional
Source University Hospital Birmingham
Contact Jamie Walton, Bsc
Phone 01213712535
Email jamie.walton@uhb.nhs.uk
Status Not yet recruiting
Phase N/A
Start date August 2023
Completion date July 2024

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