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

Completed · Not applicable

Conditions studied: Peripheral Vascular Interventions

In brief

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).

Key facts

Study ID

NCT06141694

Run by

Microbot Medical, INC

People needed

20

Starts

2024-07-02

Expected to finish

2024-10-15

Last updated by the study team

2024-10-17

Who can join

Age: 22 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• The subject is age 22-80 years at screening.
• The subject has been informed of the nature of the study and is willing and able to provide informed consent to participate in the study.
• The subject has a clinical indication for an elective PVI.
• The subject is willing and able to comply with all required study procedures.
• Subject's scheduled procedure is compatible with commercially available peripheral interventional devices that have the following diameter ranges:
• Guidewires: 0.014-0.018"
• Catheters (Microcatheters): 2-3 Fr
• Guide catheter: 4-6 Fr

You may not qualify if…

• Subject is planned to undergo coronary and/or neuro-interventional procedures during study procedure.
• Subject with vasculature that cannot accommodate the catheter or required accessories according to local routine practice guidelines.
• Subject with contraindication to endovascular approach to the treatment of peripheral vascular disease, similar or same as contraindications in manual procedures.
• Target vessel has been previously treated with any type of a bypass conduit.
• Subject has a contraindication to standard anticoagulation for PVIs.
• Subject has bleeding or a hypercoagulability disorder.
• Subject has thrombocytopenia (<50 x103 per µL).
• Subject has abnormal, clinically relevant lab results resulting in treatment and/or increased risk to the subject.
• Subject has an elevated serum creatinine (≥2.5 mg/dL or ≥221 mmol/L).
• Subject has an active infection requiring antibiotic or anti-fungal systemic treatment.
• Subject has a known allergy to any material used or any component of the devices used that will be in direct contact with subject's tissue.
• Subject is pregnant or lactating.
• Subject with any medical, social, or psychological conditions which, in the opinion of the investigator, would prohibit appropriate consent or impair completion of the study protocol or study procedures.
• Subject who is incapable, per the investigator's discretion, of following-up with the study visit schedule for any reason.
• Subject is currently participating in an investigational drug or device study or post market registry, or participated in another investigational drug or device study within one month prior to enrollment.

Where it is running

• Baptist Hospital of Miami — Miami, Florida, United States
• Brigham and Women's Hospital — Boston, Massachusetts, United States
• Memorial Sloan Kettering Cancer Center — New York, New York, United States

Full record on ClinicalTrials.gov

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