Transcatheter Aortic Valve Replacement (TAVR) Clinical Trials

Clinical trials related to Transcatheter Aortic Valve Replacement (TAVR) Procedure

Physiologic Cardiac Pacing to Prevent Left Ventricular Dysfunction Post Transcatheter Aortic Valve Implantation

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The study aims to compare permanent Conduction System Pacing (CSP) with the standard therapy - Right Ventricular Pacing (RVP) or Biventricular Pacing (BVP) - in preventing the development and progression of symptomatic Chronic Heart Failure (CHF) and improving survival in patients after Transcatheter Aortic Valve Implantation (TAVI).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• transcatheter aortic valve implantation (TAVI) in up to 30 days before qualification to pacemaker implantation

• Fulfilled criteria for permanent pacemaker implantation according do 2021 ESC guidelines

• Written informed consent

• Age of at least 18 years

Locations
Other Locations
Poland
Medical University of Silesia in Katowice
RECRUITING
Katowice
Contact Information
Primary
Krzysztof S. Gołba, MD PhD
krzysztof.golba@gmail.com
+48 (32)359-88-93
Backup
Tomasz Soral, MD
tomasz.soral@gmail.com
Time Frame
Start Date: 2024-02-27
Estimated Completion Date: 2028-06
Participants
Target number of participants: 500
Treatments
Experimental: Conduction System Pacing
Patients who receive Conduction System Pacing in form of Left Bundle Branch Area Pacing or His Bundle Pacing.
Active_comparator: Standard Pacing Method
Patients who receive currently standard pacing method with exact type of ventricular pacing depending upon left ventricular ejection fraction (LVEF): right ventricular pacing in case of LVEF \>= 40% or biventricular pacing if LVEF is determined to be less than 40%, as per current ESC guidelines.
Sponsors
Leads: Medical University of Silesia
Collaborators: Medical Research Agency, Poland

This content was sourced from clinicaltrials.gov