Clinical and echocardiographic outcomes of left bundle area pacing
Phase 4
- Conditions
- Health Condition 1: I455- Other specified heart block
- Registration Number
- CTRI/2022/10/046216
- Lead Sponsor
- Medtronic Inc
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adult patients aged > 18 years who were subjected to either,
1. permanent left bundle branch area pacing for the atrioventricular block or bundle branch
block, irrespective of the left ventricular ejection fraction (This subgroup essentially
represents the CRT-P and Brady populations.), or
2. Those who had left bundle -optimized CRT
Exclusion Criteria
1. Patients not giving consent
2. Planned for conventional pacing or any form of physiological pacing other than LBB
pacing
3. Pregnancy
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the <br/ ><br>pacing characteristics, clinical and echocardiographic outcomes of adult patients who require permanent <br/ ><br>pacemaker implantation for AV block/Bundle branch block and are taken up for conduction system pacing <br/ ><br>techniques(His bundle pacing/Left bundle branch pacing) as per their clinical considerationsTimepoint: Clinical Outcome will be accessed after 36 months(Review in every 6 months) of enrollment
- Secondary Outcome Measures
Name Time Method the composite endpoint among patients with a prespecified burden of ventricular pacing and individual outcomes.Timepoint: Clinical Outcome will be accessed after 36 months(Review in every 6 months) of enrollment