European TauroPace Registry - University of Schleswig-Holstein Prospective Observational Clinical Study
Condition(s) studied
Investigational drug(s) / intervention(s)
TauroPace™: TauroPace™ is intended to be used as a disinfecting solution during any CIED related surgery procedure or handling of any uncoated or silicon-, epoxy- or polyurethane-coated CIED (including its components, e.g., leads) made of titan or stainless steel in any adult patient requiring or carrying a CIED.
Study summary
University of Schleswig-Holstein Campus Kiel is sponsoring the European TauroPace Registry. This investigator-initiated local, prospective, non-interventional, multi-center study includes patients undergoing cardiac implantable electronic placement including and not limited to placement, revision with the aim to upgrade or downgrade, generator substitution, additional lead placement, revision or extraction (procedure) with adjunct TauroPace. It is planned to include a total of at least 2300 procedures (valid for safety analysis).
Eligibility
Primary outcome measure(s)
- CIED infections — three months
CIED infections occurring in an observation period of three months after any CIED related surgical procedure in different CIED using a regimen with surface disinfection of CIEDs and irrigation of the surgical site (pocket) with a taurolidine containing antimicrobial compound adjunct.
Trial sites (8)
| Facility | City | Region | Status |
|---|---|---|---|
| Landeskrankenhaus Wiener Neustadt | Wiener Neustadt | Austria | |
| Louis Pradel Hospital | Lyon | Bron | |
| Krankenhaus Landshut Achdorf | Landshut | Bavaria | |
| Helios Klinik Cuxhaven | Cuxhaven | Lower Saxony | |
| Helios Klinik Wesermarsch | Nordenham | Lower Saxony | |
| University Hospital Schleswig-Holstein | Kiel | Schleswig-Holstein | |
| Ospedale Regionale San Maurizio | Bolzano | Trentino-Alto Adige | |
| Great Western Hospitals NHS Foundation Trust | Swindon | United Kingdom |
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04735666 on ClinicalTrials.gov ↗ ← All trials in France