Augmented Reality For MRI-Guided Interventions
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age3-21
SponsorChildren's National Research Institute
About this trial
The purpose of this study is to determine feasibility and safety of using an augmented reality system in patients undergoing MRI-Guided needle 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 3 to 21
Patient referred to Interventional Radiology for image-guided needle injection, aspiration, or biopsy.
Disqualifiers
Patients who are unable to give informed consent themselves or through their parents.
Patients under 3 years of age
Patients over 300 pounds.
Patients who are claustrophobic and unable to tolerate MRI-guided procedure.
Trial design
Treatments tested in this trial
- Augmented Reality System
Treatment groups
25 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov