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Clinical and CPET Parameters That Predict Improvement in Functional Capacity After TAVI

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Trial details

Who runs it
Hospital Clinic of Barcelona
Trial code
NCT06833762
Record updated
2 September 2026
Original description
Determining Clinical and Cardiopulmonary exercise testing Parameters that may predict Improvement in Capacity After Transcatheter Aortic Valve ImplantationRead full original descriptionShow less

Determining Clinical and Cardiopulmonary Exercise Testing Parameters That Predict Improvement in Functional Capacity and Complications After Transcatheter Aortic Valve Implantation

Determining Clinical and Cardiopulmonary exercise testing Parameters that may predict Improvement in Capacity After Transcatheter Aortic Valve Implantation

Inclusion: All those patients ≥ 18 years of age with severe aortic stenosis approved for transfemoral TAVI; Both sexes, male and female will be included in the study.

Exclusion: Previous syncope; Previously known dynamic left ventricular outflow tract (LVOT) obstruction, defined as LVOT gradient of ≥ 30 mmHg by echocardiography; Concomitant coronary artery disease pending percutaneous coronary intervention; Proven exercise-induced arrhythmias; Very severe aortic stenosis, defined as a valve area of ≤0.6 cm2; , mean gradient ≥60 mmHg or Vmax >5 m/s; Inability to consent; Physical limitation to perform an exercise test; Non-elective procedure; Valve-in-valve procedure.

ClinicalTrials.gov NCT06833762