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

Mayo Clinic · NCT07822425

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18–90 · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
10
US sites recruiting
1
Study start
September 17, 2026
Record last updated
September 16, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Being studied: LUMENA Guidance System

Conditions: Biopsy; Ablation

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

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.

Recruiting US locations

Study contacts (from the official record)

  • Nic Dybel · 904-953-4324 · dybel.nicolas@mayo.edu
  • Julia Santos · 904-953-3280 · santos.julia@mayo.edu
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A Study Of Augmented Reality Real-Time Guidance With In-situ Feedback (NCT07822425) | Bored Studies