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Safety, Performance, and Clinical Benefit of Pacing the Left Bundle Branch Area - Post-Market Clinical Follow-up

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NCT07209852 · readout in 1,108 d

Sponsored by Boston Scientific Corporation (industry) · BSX — their whole pipeline →.

Phase
Status
Recruiting
Study type
Observational
Enrollment
140estimated
Sites
13
Countries
Belgium, France, Germany +4

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-12-19actualWhen the study began enrolling
Primary completion2029-08-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-08-31estimatedThe whole study's end, after follow-up
First posted2025-10-07actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-12actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Bradycardia
  • Atrioventricular Block
  • Sinus Node Dysfunction
  • Bundle-Branch Block

Intervention

  • Device: Pacemaker lead — also filed as Bradycardia pacemaker system, Left Bundle Branch Area Pacing (LBBAP) Lead

Primary outcomes

what the primary-completion date above is the date OF
LBBA Implant Success Rate
measured At the time of implant procedure (Day 0).
Maintenance of Ventricular Synchrony (Paced QRS Duration)
measured From implant through 3-year follow-up.

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