Prospective Use of Philips iSuite for Interventional Procedures

Part of paid clinical trials in Rochester, Minnesota.

Sponsor
Mayo Clinic
Study ID
NCT03432936
Status
Enrolling By Invitation

Conditions

  • Cancer
  • Tumor

Eligibility Criteria

Sex
ALL
Age
18 Years - 90 Years
Healthy Volunteers
Not accepted

Interventions

  • MRI guided procedure software evaluation — DEVICE
    MRI guided ablation/biopsy using standard MR imaging along with Philips Interventional iSuite software tools.

Study Details

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.

Key Dates

Start date
Jun 1, 2021
Status verified
Mar 2026
Primary completion
Dec 31, 2026
Completion
Dec 31, 2026

Study Design

Enrollment
12 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY

Arms

  • Experimental: MRI guided procedure software evaluation
    Evaluate the workflow and effectiveness of the Philips Interventional iSuite software during biopsies and/or ablations versus standard MR imaging in aiding needle placement.

Primary Outcome Measure

Needle placement efficiency into target lesion [ Time Frame: Baseline (completion of MRI-guided biopsy and /or ablation procedure) ]

Locations (1)

FacilityCityStateZIPSite coordinators
Mayo Clinic in RochesterRochesterMinnesota55905-

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Mayo Clinic in Rochester· Rochester, MN

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