Clinical Trial

QoL After Complex Endovascular Aortic Repair

Recruiting
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Summary
The goal of this prospective observational cohort study is to compare health related quality of life in patients with abdominal aortic aneurysms treated by either standard or complex EVAR (endovascular aneurysm repair) devices. The main questions it aims to answer are: * Compare differences between the physical scores from the preoperative to the postoperative settings between patients treated with standard EVAR vs non-standard endovascular aortic repair (F-/BEVAR) * To compare long-term physical scores postoperatively between patients treated with standard EVAR vs non-standard endovascular aortic repair (F-/BEVAR) at one year. * To explore at which time points (if ever) patients treated with standard-EVAR and nonstandard endovascular aortic repair (F-/BEVAR) have restored or normalized physical scores measured by SF-12, measured at 30 days, 6 months, 1 and 3 years. Participants will be asked to fill out forms pre- and postoperatively with regards to health related quality of life. The different groups for comparison will be either standard EVAR for infrarenal aortic aneurysms or complex EVAR (fenestrated or branched) for paravisceral aortic aneurysms (PVAAA).
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2023-03-07.
Trial Details
NCT Number NCT05774938
Lead Sponsor Karolinska University Hospital
Conditions Quality of Life, Aortic Aneurysm, Aortic Aneurysm, Abdominal
Enrollment 90 participants
Start Date 2023-02-28
Primary Completion 2026-12 (estimated)
Study Completion 2030-01 (estimated)
Updated on ClinicalTrials.gov 2025-04-10