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Exoskeleton vs. Standard Lead Apron in EVAR Procedures

NCT07528144 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2

Last updated 2026-08-13

No results posted yet for this study

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.

Conditions

  • Radiation Exposure to Operator
  • Endovascular Aortic Repair
  • Musculoskeletal Strain
  • Occupational Radiation Exposure

Interventions

DEVICE

Exoskeleton-supported radiation protection system

An exoskeleton-supported radiation protection system with visor used by the operator during endovascular aortic repair procedures.

DEVICE

Standard lead apron

A standard lead apron used by the operator during endovascular aortic repair procedures.

Sponsors & Collaborators

  • Samodzielny Publiczny Szpital Kliniczny nr 2 PUM

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
35 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-11-03
Primary Completion
2027-06-17
Completion
2027-06-17

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07528144 on ClinicalTrials.gov