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CArotid Robotic Procedure Evaluation

NCT05093127 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 7

Last updated 2023-05-12

No results posted yet for this study

Summary

This study aims to evaluate the use of R-One in the peripheral vasculature.

Conditions

  • Carotid Artery Diseases

Interventions

DEVICE

Carotid Artery Stenting

R-OneTM system is a tool available to physicians for performing CAS without changing the treatment of the pathology. R-OneTM system is designed to remotely deliver and manipulate guidewires and stent/balloon devices during Carotid Artery Stenting. The system is composed of the R-OneTM robotic platform used in combination with two accessories, the Mobile radioprotection screen and a sterile and single-use R-OneTM consumable kit. The physician, seated at the remote radio-protected control station, manipulates guidewires and/or balloon/stent catheters using joysticks on the Command unit.

Sponsors & Collaborators

  • European Cardiovascular Research Center

    collaborator NETWORK

  • Robocath

    lead INDUSTRY

Principal Investigators

  • François EUGENE, MD · Rennes University Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-11-16
Primary Completion
2022-11-15
Completion
2022-11-15

Countries

  • France

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 NCT05093127 on ClinicalTrials.gov