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ENROLLING BY INVITATION
NCT07752251
NA

A Study Of Subscalp Placement Of The LINQII Device

Sponsor: Mayo Clinic

View on ClinicalTrials.gov

Summary

The purpose of this to evaluate the capability of the FDA approved Medtronic LINQ II device (implantable cardiac monitoring device) to record EEG signals when placed temporarily in the subscalp space in patients undergoing cranial neurosurgery. No disease-directed therapeutic efficacy endpoints will be studied.

Official title: Subscalp Placement Of The LINQII Device: A First-in-human Device Feasibility Study

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

10

Start Date

2026-11

Completion Date

2027-11

Last Updated

2026-08-07

Healthy Volunteers

No

Interventions

DEVICE

Medtronic LINQII

Bilateral LINQII devices will be implanted under the scalp during surgery to obtain approximately 30 minutes of brain signal recordings.

Locations (1)

Mayo Clinic in Arizona

Scottsdale, Arizona, United States