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Assessment of Clin. Capabilities of LIBERTY® Endovascular Robotic System's Performance & Safety in Periph. Vasc. Interv.

NCT06141694 · Microbot Medical, INC · Updated 17 Oct 2024

What is being tested
The LIBERTY® Robotic System
For
Peripheral Vascular Interventions
Kind of study
Tests a treatment or device on volunteers. No drug phase (a device or procedure study).
Who can join
Ages 22 years to 80 years. About 20 people. The full rules are on the registry page.
Where
United States (3 sites)
When
Starts or started 2 July 2024, ends 15 Oct 2024. Registered 21 Nov 2023.
Results
None posted yet.

In the researchers' words

A prospective, multi-center, single-arm, study to evaluate the performance and safety of the LIBERTY® Robotic System in human subjects undergoing Peripheral Vascular Interventions. The study is designed to evaluate the performance and safety of endovascular procedures supported by the LIBERTY® Robotic System. The System is configured to deliver and manipulate third-party commercially available surgical devices that are employed in endovascular transcatheter procedures (guidewires, microcatheters, and guiding catheters).
ClinicalTrials.gov, NCT06141694

Sites

  • Baptist Hospital of MiamiMiami, Florida, United States
  • Brigham and Women's HospitalBoston, Massachusetts, United States
  • Memorial Sloan Kettering Cancer CenterNew York, New York, United States