U.S., Feb. 7 -- ClinicalTrials.gov registry received information related to the study (NCT07393009) titled 'Studying Routine Patient Care With BIOTRONIK Devices That Allow a More Natural Heart Stimulation' on Jan. 09.
Brief Summary: The registry is designed to assess outcome, performance and residual safety aspects of BIOTRONIK products which are used in the context of CSP based on long-term data from an unselected, real-life clinical set-up.
Study Start Date: March 01
Study Type: OBSERVATIONAL
Condition:
Cardiac Pacing
Cardiac Pacemaker
Implantable Cardioverter Defibrillator
Cardiac Resynchronization Therapy Devices
Bradycardia
Tachycardia
Heart Failure
Intervention:
DEVICE: Implantation of the Solia CSP S pacing lead for LBBAP
Obs...