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

Augmented Reality Real-Time Guidance With In-situ Feedback

Who can join

Ages 18 to 90 · All sexes · Healthy volunteers welcome

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.

About the study

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.

What is being tested

• LUMENA Guidance System (device)

Sponsor: Mayo Clinic · Participants: 10 · Started: Sep 17, 2026

Contact the study team

• Nic Dybel · Phone: 904-953-4324
• Julia Santos · Phone: 904-953-3280

Official record on ClinicalTrials.gov — NCT07822425

Locations in the U.S.

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.