Aortic Valve Stenosis Clinical Trials

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Effects of Post-Dilatation on THV Expansion, Hemodynamics, Durability, and Outcomes in Balloon-Expandable TAVI Prostheses

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

Asymmetrical and inadequate expansion of transcatheter heart valves (THVs) have been described as a key predictor of impaired valve hemodynamic performance predisposing patients for bioprosthetic valve dysfunction (BVD) and death. Post-dilatation using the original delivery system balloon at the identical filling volume after deployment of balloon-expandable THVs represents an invasive strategy to potentially optimize expansion and reduce asymmetry of balloon-expandable THVs. Currently, the efficacy and safety of routine post-dilatation has never been assessed in a randomized controlled fashion. The present randomized controlled DUOTAP trial aims to assess efficacy and safety of routine post-dilatation on THV expansion, hemodynamics, durability, and associated clinical outcomes in patients with severe aortic stenosis.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 65
Healthy Volunteers: f
View:

• Severe AS

• AS treatment by transfemoral TAVI as determined by an interdisciplinary heart team board

• Anatomical feasibility to receive a balloon-expandable THV

• Age 65 years or older

• Informed consent

Locations
Other Locations
Austria
Medical University of Vienna
RECRUITING
Vienna
Contact Information
Primary
Christian Nitsche, MD, PhD
christian.nitsche@meduniwien.ac.at
+43-1-40400-48590
Backup
Philipp E Bartko, MD, PhD
philippemanuel.bartko@meduniwien.ac.at
+43-1-40400-48590
Time Frame
Start Date: 2025-01-01
Estimated Completion Date: 2031-05
Participants
Target number of participants: 146
Treatments
No_intervention: No post-dilatation after THV deployment
Experimental: Nominal post-dilatation using the original delivery balloon
Related Therapeutic Areas
Sponsors
Leads: Medical University of Vienna

This content was sourced from clinicaltrials.gov