Clin2
NCT07528144Likely a fitRecruiting

Exoskeleton vs. Lead Apron for Surgeon Protection During Aortic Repair

Radiation Exposure to OperatorEndovascular Aortic RepairMusculoskeletal StrainOccupational Radiation Exposure

Part of Bones, joints & muscles, Heart & circulation, Injuries & trauma clinical trials.

This study compares a new exoskeleton device (a wearable support system) to standard lead aprons for protecting surgeons from radiation during endovascular aortic repair procedures—a minimally invasive surgery to fix problems in the main artery in the abdomen. The trial tests whether the exoskeleton provides better protection and comfort.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
2 people
Ages
35 years and older
Study type
Interventional

Who can take part

  • You must be a vascular surgeon (a doctor who specializes in blood vessel surgery) with significant experience performing endovascular procedures
  • You must actively participate in endovascular aortic repair procedures as either the primary surgeon or an assistant
  • You must have a high volume of endovascular procedures in your practice
  • You must be at least 35 years old
  • You must be able to provide written informed consent and understand the study procedures
  • You cannot have medical conditions that would make wearing a lead apron or exoskeleton unsafe for you

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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