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ECG and Echo Characteristics of BBAP

Electrocardiographic and Echocardiographic Characteristics of Bachmann's Bundle Area Pacing

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06995027
Acronym
BBAP-ECG/echo
Enrollment
31
Registered
2025-05-29
Start date
2024-08-31
Completion date
2025-12-31
Last updated
2026-05-20

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

Conditions

Cardiac Pacing, Pacing Therapy

Keywords

Bachmann's bundle pacing, Bradycardia, Physiological pacing

Brief summary

This is a prospective, single-site, non-randomized, interventional study. The purpose is to collect electrocardiographic (ECG) and echocardiographic (echo) parameters and computed tomography (CT) images (optional) during Bachmann's bundle area pacing (BBAP) and conventional pacing in the right atrial appendage (RAA) to compare the differences between atrial pacing modalities and to further investigate the clinical outcomes of BBAP.

Detailed description

Bachmann's bundle (BB) has emerged as an alternative pacing location to conventional right atrial appendage (RAA) pacing and is expected to avoid the interatrial conduction delay (IACD) and atrial dyssynchrony induced by RAA pacing. A recent study reported in patients with atrial pacing indications and baseline IACD that decreased atrial arrhythmia burden, recurrence, and de novo incidence were found in BB pacing, compared with right atrial septal pacing and RAA pacing. This study aimed to collect electrocardiographic (ECG) and echocardiographic (echo) parameters and CT images during BB area pacing (BBAP) and conventional pacing in the right atrial appendage (RAA) during regular pacemaker implantation procedures. The purpose is to compare the differences between atrial pacing modalities and to further investigate the clinical outcomes of BBAP.

Interventions

PROCEDUREBBAP and RAA pacing

Bachmann's bundle area pacing and conventional pacing in the right atrial appendage during regular pacemaker implantation procedures are applied for acute electrocardiogram and echocardiogram testings.

Sponsors

Shanghai Tong Ren Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients aged \>= 18 years old * Patients who are willing to provide Informed Consent * Patients who are indicated to atrial pacing, dual-chamber pacing, or cardiac resynchronization therapy * Patients who consent to Bachmann's bundle area pacing

Exclusion criteria

* Patients who are indicated for cardiac implantable electronic device replacement or upgrade * Patients with defibrillation indications * Patients who are pregnant or have a plan for pregnancy during the study * Patients who have medical conditions that would limit study participation * Patients who were already enrolled in other trials which would impact his/her participation

Design outcomes

Primary

MeasureTime frame
Atrial-paced ECG P-wave duration at implantation and during regular follow-upsFrom implantation to regular follow-ups up to 6 months
Atrial-paced ECG P-wave amplitude at implantation and during regular follow-upsFrom implantation to regular follow-ups up to 6 months
Atrial-paced P-onset to A-wave initiation time under Doppler at mitral and tricuspid valves at implantationPerioperative

Secondary

MeasureTime frame
LAD from echocardiographic measurements before implantation and during regular follow-upsBaseline before implantation to regular follow-ups up to 6 months

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 21, 2026