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NCT07209852: SEPTA PMCF

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

Recruiting now Last updated 3 April 2026
What this trial tests

trial testing Pacemaker lead in Bradycardia in 140 participants. Currently enrolling.

Timeline
19 December 2025
Primary endpoint
31 August 2029
31 August 2029

Quick facts

Lead sponsorBoston Scientific Corporation
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment140
Start date19 December 2025
Primary completion31 August 2029
Estimated completion31 August 2029
Sites13 locations across France, Italy, Belgium, United Kingdom, Germany, Switzerland, Spain

Drugs / interventions tested

Conditions studied

Sponsor

Boston Scientific Corporation — full company profile →

Who can join

18 and older, any sex, with Bradycardia or Atrioventricular Block. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this observational post-market clinical Follow-up study is to learn about the long-term safety, performance, and clinical benefits of pacing the left bundle branch area (LBBAP) using the INGEVITY+ pacemaker lead in patients with bradycardia who need a pacemaker.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Bradycardia

Currently open trials in the same condition.

Other Boston Scientific Corporation trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07209852.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing