Clinical and echocardiographic outcomes of left bundle area pacing

"CLINICAL AND ECHOCARDIOGRAPHIC OUTCOMES AFTER CONDUCTION SYSTEM PACING: A MULTI-CENTRIC OBSERVATIONAL STUDY"

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2022/10/046216

Enrollment

200

Registered

2022-10-06

Start date

Unknown

Completion date

Unknown

Last updated

2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I455- Other specified heart block

Interventions

None listed

Eligibility

Inclusion criteria

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

Exclusion criteria: 1. Patients not giving consent 2. Planned for conventional pacing or any form of physiological pacing other than LBB pacing 3. Pregnancy

Design outcomes

Primary

Measure	Time frame
the pacing characteristics, clinical and echocardiographic outcomes of adult patients who require permanent pacemaker implantation for AV block/Bundle branch block and are taken up for conduction system pacing 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	—

Measure

Time frame

the pacing characteristics, clinical and echocardiographic outcomes of adult patients who require permanent pacemaker implantation for AV block/Bundle branch block and are taken up for conduction system pacing 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

Measure	Time frame
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	—

Countries

India

Contacts

Public ContactSreelekshmiM

Sree Chitra Tirunal Institute for Medical Sciences and Technology,Trivandrum

kknnamboodiri@gmail.com9447223340

Outcome results