Clinical Trial

IOPS Technology During Cannnulation of Contralateral Limb in EVAR

Study acronym: IOPS
Not Yet Recruiting
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Record status
This record was last updated November 20, 2024 (before its estimated September 8, 2025 completion). Its status may not reflect the trial's current state.
Summary
Short-term results are favorable for EndoVascular Aneurysm Repair (EVAR) compared to open surgery. One of the major drawbacks to this shift is the need for fluoroscopy and contrast dyes to visualise endovascular devices. The use of fluoroscopy exposes both patients and caregivers to harmful ionizing radiation. Because of the harmful effects of radiation, recent radiation protection guidelines strongly recommend as low as reasonably achievable (ALARA) principle. The need for additional radiation-reducing navigation techniques is high, with the ultimate goal of performing endovascular procedures without radiation at all. In response to these challenges, Centerline Biomedical (Cleveland, Ohio, USA) has developed a proprietary electromagnetic tracking and positioning system called the Intra-Operative Positioning System (IOPS). This medical device provides surgeons with 3D visualization for increased surgical precision while reducing the radiation exposure for patients and healthcare professionals. IOPS provides 3D electromagnetic navigation of interventional devices as an adjunct to fluoroscopy. During the intervention, the IOPS devices can be visualized with on-screen image guidance. The IOPS guidewires and catheters can be used together or combined with off-the-shelf 0.035-inch catheters and guidewires, as needed. This study aims to describe the influence of IOPS technology on radiation exposure during cannulation of the contralateral limb (CL) during standard EVAR.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-08-22.
Trial Details
NCT Number NCT06570785
Lead Sponsor Clinical Centre of Serbia
Collaborators: Centerline Biomedical, Inc.
Conditions Abdominal Aortic Aneurysm, Abdominal Aortic Aneurysm Without Rupture, Radiation Exposure
Enrollment 80 participants
Start Date 2025-01-20
Primary Completion 2025-09-08 (estimated)
Study Completion 2025-11-03 (estimated)
Updated on ClinicalTrials.gov 2024-11-20