Symptomatic Aortic Stenosis

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Review clinical trials related to Symptomatic Aortic Stenosis. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Structured Shared Decision Making for Patients Undergoing SAVR or TAVR

Transcatheter aortic valve replacement (TAVR) is a well-established alternative to surgical aortic valve replacement (SAVR) for the treatment of patients with severe aortic stenosis regardless of surgical risk. While TAVR and SAVR share some of the benefits and risks, they importantly differ with regards to invasiveness, time to recovery, hemodynamics, as well as options for re-intervention and possibly valve durability. An early benefit of TAVR may be offset by late risks. Therefore, current guidelines of the European Society of Cardiology recommend an integration of patient values and preferences for the selection of the treatment modality. The objective of the TOGETHER trial is to investigate the efficacy of a structured shared decision making approach (SDM) to improve patient-centered outcomes for the choice between SAVR and TAVR. TOGETHER is an investigator-initiated, randomized, open-label, single-center clinical trial. A total of 140 patients referred for treatment of symptomatic severe aortic stenosis and deemed to undergo TAVR or SAVR according to heart team decision will be randomized in a 1:1 ratio to structured SDM or usual care.

Participants needed: 140
Trial details
Age: 70+Biological sex: AllType: InterventionalSponsor: Insel Gruppe AG, University Hospital BernUpdated: May 8, 2026Locations: 1
Eligibility criteria

Age ≥ 70 years [+2]

Life expectancy <1 year irrespective of valvular heart disease [+2]

Status: Recruiting

Pivotal Study of the Vienna Transcatheter Self Expandable Aortic Valve SE System

This is a prospective, single arm, multicenter study in an cohort of up to 267 patients (up to 100 Roll-ins and 167 patients implanted per protocol) symptomatic patients with severe aortic stenosis who will be followed up for up to 5 years.

Participants needed: 267
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: P+F Products + Features GmbHUpdated: Jun 29, 2025Locations: 31
Eligibility criteria

Male or Female [+15]

Patient has a congenital unicuspid or bicuspid aortic valve or non-calcified val... [+34]

Status: Recruiting

Transcatheter Aortic Valve Replacement Single Center Registry in Chinese Population

The purpose of this study is to evaluate the safety and effectiveness of transcatheter aortic valve replacement in Chinese population.

Participants needed: 2,000
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Second Affiliated Hospital, School of Medicine, Zhejiang UniversityUpdated: Jul 15, 2021Locations: 1
Eligibility criteria

Patients with symptomatic aortic stenosis/regurgitation [+3]

A known hypersensitivity or contraindication to any of the following which canno... [+3]