Prospective Use of Philips iSuite for Interventional Procedures

Last updated: March 3, 2025
Sponsor: Mayo Clinic
Overall Status: Active - Enrolling

Phase

N/A

Condition

Cancer

Carcinoma

Treatment

MRI guided procedure software evaluation

Clinical Study ID

NCT03432936
17-007674
  • Ages 18-90
  • All Genders

Study Summary

This research study is being done to look at new MRI imaging guidance software, Philips Interventional iSuite software, to see if using will improve the physician's ability to quickly place and guide needle tip position for biopsies and ablations.

Eligibility Criteria

Inclusion

Inclusion criteria:

  • Patients already scheduled for a percutaneous MR guided procedure

Exclusion

Exclusion criteria:

  • Pregnant Women

Study Design

Total Participants: 12
Treatment Group(s): 1
Primary Treatment: MRI guided procedure software evaluation
Phase:
Study Start date:
June 01, 2021
Estimated Completion Date:
December 31, 2026

Study Description

The purpose of this study is to evaluate Philips Interventional iSuite software used for MRI guided procedures in the MRI suite. The real-time MRI Imaging software will be used during an MRI procedure to take continuous pictures.

The Philips Interventional iSuite software package has not received FDA 510(k) clearance. The Investigator will be evaluating and publishing on the use of this software as a clinical aid in performing interventional procedures within the MR suite. The primary evaluation will be weighted toward enhanced facilitation of ablation procedures. However, the software will not replace standard MR imaging for final confirmation of needle tip position and ablation margins.

Connect with a study center

  • Mayo Clinic in Rochester

    Rochester, Minnesota 55905
    United States

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.