Augmented Reality Guidance with Real-Time Feedback for CT-Guided Biopsy/Ablation

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study evaluates the feasibility and safety of the LUMENA guidance system when used during CT-guided needle placement for biopsy or ablation of various organs. Participants are adults aged 18 to 90 who require CT-guided procedures and can provide informed consent. The study focuses on real-time augmented reality guidance with in-situ feedback to support interventional radiologists during procedures. No efficacy endpoints are listed beyond feasibility and safety. The Mayo Clinic is the lead site for this trial, with no other collaborators.

Why it matters

Who can join: the full rules

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.

Where it's running

• Mayo Clinic
  Jacksonville, Florida, United States Recruiting

Study contacts

• Principal investigator: David Sella, MD — Mayo Clinic
• Study coordinator: Nic Dybel
• Email: dybel.nicolas@mayo.edu
• Phone: 904-953-4324

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.