Exoskeleton vs. Standard Lead Apron in EVAR Procedures
The goal of this clinical trial is to learn whether an exoskeleton-supported radiation protection system can reduce radiation exposure and musculoskeletal strain in vascular surgeons during endovascular aortic repair procedures, compared with standard lead aprons. Researchers will compare procedures performed with exos
| Condition(s) | Radiation Exposure to Operator, Endovascular Aortic Repair, Musculoskeletal Strain, Occupational Radiation Exposure |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | The goal of this clinical trial is to learn whether an exoskeleton-supported radiation protection system can reduce radiation exposure and musculoskeletal strain in vascular surgeons during endovascular aortic repair procedures, compared with standard lead aprons. Researchers will compare procedures performed with exoskeleton-supported protection and procedures performed with standard lead aprons. Radiation exposure, physical strain, fatigue, and discomfort will be assessed during and after procedures. |
| Who can participate | Inclusion Criteria: * age 35 years or older * written informed consent obtained * vascular surgeon with substantial experience in endovascular procedures * active participation in endovascular aortic repair procedures as a primary operator or assistant * high procedural volume in endovascular interventions Exclusion Criteria: * refusal or inability to provide informed consent * medical contraindications to the use of standard lead aprons or the exoskeleton-supported radiation protection system * health conditions preventing safe participation in study procedures |
| Ages | 35 Years |
| Sex | All |
| Accepts healthy volunteers | Yes |
| Lead sponsor | Samodzielny Publiczny Szpital Kliniczny nr 2 PUM |
| Locations | Szczecin, West Pomeranian Voivodeship, Poland |
| Start date | 2025-11-03 |
| NCT ID | NCT07528144 |
| Official listing | https://clinicaltrials.gov/study/NCT07528144 |