UHF ECG in LBBB and Response to CRT Prediction

Recruiting N/A Interventional Study
Left Bundle Branch Block Left Bundle Branch Area Pacing Biventricular Pacing Intraventricular Conduction Delay
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
200 (estimated)
Sponsor
Faculty Hospital Kralovske Vinohrady · Government
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About This Trial
The main objective of the project is to demonstrate that in patients with heart failure and QRS complex of nonRBBB morphology lasting over 130 ms, UHF-ECG can differentiate patients with trueLBBB from IVCD better than existing approaches based on the assessment of QRS complex morphology and duration from 12-lead ECG. Another goal of the proposed study is to demonstrate that trueLBBB patients will…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * HF due to ischemic or non-ischemic cardiomyopathy * known coronary angiography * NYHA II-IV * LVEF ≤40% * non-RBBB QRSd lasting \>130 ms (by automated measurement) * proximal LBBB proved by an invasive EP study or non-invasive dyssynchrony assessment in case such a method is c…
Contacts

Karol Curila, MD

+420777869171

karol.curila@fnkv.cz

CONTACT