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Search / Trial NCT07046832

Clinical Evaluation of an Augmented Reality Intraprocedural Needle Guidance Platform for Soft Tissue Biopsy

Launched by MEDIVIEW XR, INC. · Jul 1, 2025

Trial Information

Current as of July 22, 2025

Enrolling by invitation

Keywords

Percutaneous Interventions Needle Guidance Augmented Reality Medical Device Xr90 Minimally Invasive

ClinConnect Summary

This clinical evaluation is needed to further characterize and quantify the potential benefits of percutaneous biopsy, assisted with the XR90 3D surgical imaging system. This continued innovative implementation of the platform as a medical device to assist in percutaneous targeted biopsy of soft tissue tumors will allow for further assessment of device functionality, operator acceptability, and additional data collection to help quantify the potential benefits of this platform. Potential benefits to the patient, to be formally proven in future studies: decreased procedure time, decreased of...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • At least 18 years of age
  • Willing and able to give informed consent prior to enrollment
  • Subjects in need of a diagnostic soft-tissue tumor biopsy which is the primary target for needle placement as a part of their standard of care.
  • Subjects who have met all criteria to undergo percutaneous biopsy with ultrasound.
  • Subjects with soft-tissue lesions ≥1 cm or ≤8 cm in depth
  • BMI of ≤40
  • Exclusion Criteria:
  • Children under the age of 18.
  • Currently pregnant at the time of the procedure
  • Not willing or able to give informed consent.
  • Subjects with pacemakers or AICDs.

About Mediview Xr, Inc.

Mediview XR, Inc. is a clinical research organization specializing in the development and management of advanced extended-release pharmaceutical formulations. Committed to improving patient outcomes, Mediview XR focuses on innovative drug delivery technologies and rigorous clinical trial execution to bring safer, more effective therapies to market. Their expertise spans multiple therapeutic areas, emphasizing quality, compliance, and scientific integrity throughout the research process.

Locations

New York, New York, United States

Washington, District Of Columbia, United States

Washington, District Of Columbia, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported