Augmented Reality Real-Time Guidance for MRI-Guided Interventions
ConditionLiver
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-90
SponsorMayo Clinic
About this trial
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.
Eligibility criteria
Qualifiers
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.
Disqualifiers
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.
Trial design
Treatments tested in this trial
- MRI guided procedure software evaluation
Treatment groups
20 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov