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

Part of paid clinical trials in Jacksonville, Florida.

Sponsor
Mayo Clinic
Study ID
NCT07822425
Status
Recruiting
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Conditions

  • Ablation
  • Biopsy

Eligibility Criteria

Sex
ALL
Age
18 Years - 90 Years
Healthy Volunteers
Accepted

Interventions

  • LUMENA Guidance System — DEVICE
    LUMENA is an augmented reality needle guidance system that provides real-time visual guidance during CT-guided needle placement procedures.

Study Details

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.

Key Dates

First listed
Sep 16, 2026
Start date
Sep 17, 2026
Status verified
Sep 2026
Primary completion
Sep 16, 2028
Completion
Sep 16, 2028

Study Design

Enrollment
10 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY

Arms

  • Experimental: LUMENA Augmented Reality Guidance
    Participants will undergo clinically indicated CT-guided needle placement for ablation or biopsy with use of the LUMENA augmented reality guidance system.

Primary Outcome Measure

Feasibility of completing the CT-guided needle placement procedure using the LUMENA guidance system [ Time Frame: 2 years ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Mayo ClinicJacksonvilleFlorida32224
Riley Nichols
904-953-7783
David Sella, MD (PRINCIPAL_INVESTIGATOR)

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