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Prediction of Long-term Outcome in Aortic Stenosis After Valve Intervention

U

Uppsala University

Status

Enrolling

Conditions

Aortic Stenosis

Treatments

Other: There is no intervention since it is an observational study patients are treated according to clinical praxis

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Patients with severe aortic stenosis accepted for transcatheter intervention or open surgery are included before the intervention, and then followed up with clinical visits during the first year after intervention. Imaging with echocardiography and computed tomography (CT) are performed together with additional imaging with magnetic resonance imaging (MRI) and Positron emissions tomography (PET)-CT in a subgroup of the study population. Blood samples, physical performance and questionnaires with focus on frailty and heart failure are also collected at each visit. A follow up with information of the outcomes after 2-5 years will be performed through national registries.

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Accepted for aortic valve intervention

Exclusion criteria

  • No able to follow the study protocol

Trial design

300 participants in 2 patient groups

Preserved heart function
Description:
The group will be defined as preserved left ventricular ejection fraction (LVEF) with and without hypertrophy and with and without reduced global longitudinal strain (GLS).
Treatment:
Other: There is no intervention since it is an observational study patients are treated according to clinical praxis
Reduced heart function
Description:
The group will be defined as reduced LVEF
Treatment:
Other: There is no intervention since it is an observational study patients are treated according to clinical praxis

Trial contacts and locations

1

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Central trial contact

Christina Christersson, MD PhD

Data sourced from clinicaltrials.gov

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