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RECRUITING
NCT04804748

The DefiPace Study

Sponsor: Institut für Pharmakologie und Präventive Medizin

View on ClinicalTrials.gov

Summary

Prospective, non-interventional, multi-center, international registry in two phases in consecutive patients undergoing elective cardiac surgery. The DefiPace registry is designed in two phases 1. to document the standard of care in 50 patients with atrial fibrillation (AF) 2. to assess the treatment and outcomes of patients with post-operative atrial fibrilllation using low-energy cardioversion and subsequent bi-atrial pacing in clinical practice in 100 patients

Official title: Safety and Efficacy of Low-energy Electrical Cardioversion With or Without Bi-atrial Pacing in Patients With Post-operative Atrial Fibrillation in a Real World Setting - The DefiPace Study

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

450

Start Date

2023-03-28

Completion Date

2026-08-31

Last Updated

2026-03-30

Healthy Volunteers

Not specified

Interventions

OTHER

No intervention

no intervention

Locations (10)

Medical University of Vienna

Vienna, Austria

Universitätsklinikum Erlangen

Erlangen, Bavaria, Germany

Klinikum Nürnberg

Nuremberg, Bavaria, Germany

University Hospital of Würzburg

Würzburg, Bavaria, Germany

Oldenburg Hospital AöR / Medical Campus University of Oldenburg

Oldenburg, Lower Saxony, Germany

Heart Center Dresden GmbH University Hospital

Dresden, Saxony, Germany

Albert-Ludwigs-Universitaet Freiburg

Freiburg im Breisgau, Germany

Hannover Medical School

Hanover, Germany

University Hospital Jena

Jena, Germany

University Hospital Ulm

Ulm, Germany