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Completed Not applicable Interventional Results available

BIOTRONIK Conduction System Pacing With the Solia Lead

ClinicalTrials.gov ID: NCT05251363

Public ClinicalTrials.gov record NCT05251363. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 1, 2026, 2:18 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of the BIO-CONDUCT study is to demonstrate the safety and effectiveness of the BIOTRONIK Solia S pacing lead when implanted in the left bundle branch (LBB) area. Safety will be assessed by evaluating serious adverse device effects that occur through 3 months post-implant. Efficacy will be assessed by evaluating implant success rate.

Study identification

NCT ID
NCT05251363
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Biotronik, Inc.
Industry
Enrollment
194 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 11, 2022
Primary completion
Jan 8, 2024
Completion
Oct 7, 2024
Last update posted
Mar 17, 2025

2022 – 2024

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Banner - University Medical Center Phoenix Phoenix Arizona 85006
Cardiology Associates Medical Group Ventura California 93003
Washington Hospital Center Washington D.C. District of Columbia 20010
Sarasota Memorial Health Care System Sarasota Florida 34239
Tampa General Hospital Tampa Florida 33606
Rush University Medical Center Chicago Illinois 60612
University of Chicago Chicago Illinois 60637
Cardiology Associates Tupelo Mississippi 38801
NYU Langone Health New York New York 10016
Weill Cornell Medicine New York New York 10021
Wake Forest University Health Sciences Winston-Salem North Carolina 27157
Cardiology Consultants of Philadelphia Philadelphia Pennsylvania 19107
Geisinger Wilkes-Barre Pennsylvania 18711
Medical University of South Carolina (MUSC) Charleston South Carolina 29425

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05251363, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 17, 2025 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05251363 live on ClinicalTrials.gov.

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