Clinical trials

3

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Prospective, Long-term Evaluation of the SAPIEN 3 Ultra RESILIA Valve

Evaluation of clinical outcomes and valve performance of the SAPIEN 3 Ultra Resilia (S3UR) valve over 10 years.

Participants needed: 500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Institut für Pharmakologie und Präventive MedizinUpdated: Jul 30, 2026Locations: 1
Eligibility criteria

Adult patients (≥18 years) [+2]

Lack of written informed consent [+13]

Status: Recruiting

The DefiPace Study

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

Participants needed: 450
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Institut für Pharmakologie und Präventive MedizinUpdated: Jul 30, 2026Locations: 10
Eligibility criteria

Patient is scheduled to undergo elective open chest cardiac surgery (bypass and... [+5]

Clinical history of either permanent, persistend or paroxysmal atrial fibrillati... [+5]

Status: Recruiting

The ReTAVI Prospective Observational Registry

Patients with severe aortic stenosis (sAS) treated with transcatheter aortic valve implantation (TAVI) (increasingly younger \& lower risk pts) are experiencing SVD of the index THV and thus developing an indication for a redo-TAVI procedure. The evidence on redo-TAVI (where a transcatheter heart valve \[THV\] is implanted into another THV) is limited, with initial data showing acceptable safety as well efficacy in highly selected and limited populations. Aim is to evaluate short- and long-term data on patients undergoing transcatheter redo-TAVI procedures with THVs for failure of a previously implanted THV and to determine VARC-3 defined efficacy and safety at 30 days and functional outcome at 1 year, 3 years and 5 years.

Participants needed: 250
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Institut für Pharmakologie und Präventive MedizinUpdated: Aug 20, 2025Locations: 62Duration: 5 Years
Eligibility criteria

Consenting adult patient (≥18 years) [+5]

Patients without signed informed consent / data protection statement (according... [+3]