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Active Not RecruitingNCT06620237

BIO|MASTER.CSP Study

Pivotal Study of the Amvia Pacemaker and Solia CSP S Pacing Lead on Conduction System Pacing

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
152 (estimated)
Sponsor
Biotronik SE & Co. KG · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical study is to test the clinical safety and performance of the Amvia pacemakers and the Solia CSP S lead when used for left bundle branch area pacing (LBBAP). The patient population consist of patients with cardiac pacemaker indication or cardiac resynchronization therapy indication and intended for implantation of a system with left bundle branch area stimulation. Participants will visit sites at enrollment in the study, at implantation and pre-hospital discharge, 1-, 6- and 12-month follow-up visits. Additional annual follow-up(s) may apply until study termination after regulatory approval of Solia CSP S. The total duration of the clinical investigation is expected to be until September 2027, with last patient out (LPO). During the visits the regular pacemaker and lead measurement are performed. A 12-lead ECG is recorded to document intrinsic and ventricularly paced heart rhythm to assess left bundle branch area pacing. Programming of the pacemakers will be done according to the participant´s therapeutical needs. The study will be conducted in approximately 18 sites in Europe, Australia and New Zealand where more than one physician per site are expected to participate.

Conditions

Interventions

TypeNameDescription
DEVICEImplantation of the Solia CSP S pacing lead for LBBAPLeft bundle branch area pacing using a Solia CSP S lead

Timeline

Start date
2024-10-04
Primary completion
2026-04-01
Completion
2027-09-01
First posted
2024-10-01
Last updated
2025-11-18

Locations

14 sites across 5 countries: Australia, Belgium, France, Netherlands, New Zealand

Source: ClinicalTrials.gov record NCT06620237. Inclusion in this directory is not an endorsement.