Augmented Reality Real-Time Guidance for MRI-Guided Interventions

Recruiting now · Not applicable

Conditions studied: Liver

In brief

The purpose of this research is to evaluate the safety and feasibility of using a needle guidance system (LUMENA) create by CLEAR GUIDE MEDICAL for needle placement for biopsy or liver tumor ablation procedures.

Key facts

Study ID

NCT07120906

Run by

Mayo Clinic

People needed

20

Starts

2025-07-25

Expected to finish

2026-12-31

Last updated by the study team

2026-06-26

Who can join

Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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 image-guided liver needle placement for ablation/biopsy.

You may not qualify if…

• Patients who are unable to give informed consent themselves or through their parents.
• Patients that do not fit into MR scanner (70 cm bore) with room for needle placement.
• Contraindications to MRI such as MR-unsafe implants.

Where it is running

• Mayo Clinic — Rochester, Minnesota, United States (enrolling)
• Mayo Clinic in Florida — Jacksonville, Florida, United States

Full record on ClinicalTrials.gov

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