Trials / Recruiting
RecruitingNCT06436053
Acute Response to Left Bundle Branch Area Pacing With SyncAV
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 50 (estimated)
- Sponsor
- Abbott Medical Devices · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This clinical investigation is a prospective, single-arm, post-market, non-randomized, single-center study designed to evaluate the effectiveness of the SyncAV CRT dynamic atrioventricular (AV) delay feature when used with left bundle branch area pacing (LBBAP).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | LBBAP with SyncAV | Acute changes in surface ECG QRS duration resulting from left bundle branch area pacing using various pacing configurations will be evaluated. |
Timeline
- Start date
- 2024-05-15
- Primary completion
- 2026-05-15
- Completion
- 2026-07-15
- First posted
- 2024-05-30
- Last updated
- 2025-02-21
Locations
1 site across 1 country: Italy
Source: ClinicalTrials.gov record NCT06436053. Inclusion in this directory is not an endorsement.