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Study identifier: NCT05774938 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

QoL After Complex Endovascular Aortic Repair

Condition: Quality of Life · Aortic Aneurysm · Aortic Aneurysm, Abdominal  ·  Sponsor: Karolinska University Hospital

PhaseN/A
Planned participants90
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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).

This description comes directly from the study's public registry record.

Talk to the study team

Rebecka Hultgren, MD, PhD  ·  +46 8 123 700 00  ·  rebecka.hultgren@ki.se

Mårten Huss, MD  ·  +46 8 123 700 00  ·  marten.huss@ki.se

Always discuss trial participation with your own doctor first.

Locations (1)

Karolinska University HospitalStockholm, SwedenRecruiting

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Source record: clinicaltrials.gov/study/NCT05774938