NCT07822425NARecruitingAccepts Healthy Volunteers

A Study Of Augmented Reality Real-Time Guidance With In-situ Feedback

Mayo Clinic

Start Date

9/17/2026

Completion Date

9/16/2028

Summary

The purpose of this study is to evaluate the feasibility and safety of using the LUMENA guidance system during clinical procedures in patients undergoing CT-guided needle Placement for kidney, liver, lymph node, abdominal mass and lung ablation/biopsy.

Eligibility Criteria

Age Range: 18 years to 90 years

INCLUSION CRITERIA * Provision of signed and dated informed consent form * Stated willingness to comply with all study procedures and availability for the duration of the study * Male or female, ages 18-90 years * Patient referred to Interventional Radiology for CT-guided needle placement for ablation/biopsy. EXCLUSION CRITERIA * Patients who are unable to give informed consent themselves or through their parents. * Patients that do not fit into the gantry of the CT scanner. * Patients who are sensitive to radiation exposure such as pregnant women.

Interventions

DEVICE

LUMENA Guidance System

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Conditions

BiopsyAblation

Locations

Mayo Clinic

Jacksonville, Florida 32224

United States

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