A Study Of Intraoperative Neurophysiologic Biomarkers Of Spinal Cord Stimulator Lead Placement

Overview

About this study

The purpose of this study is to determine if intraoperative electromyography (EMG) mapping of spinal cord stimulation (SCS) leads can be a valid substitute for paresthesia's to confirm accurate lead placement.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Plan for thoracic SCS paddle lead placement.

  • ≥ 18 years on the day of surgery.

Exclusion Criteria:

  • Prior SCS lead placement.

  • Spinal cord injury.

  • Lower limb amputee.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 6/23/2025. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Ernest Hoffman

Open for enrollment

Contact information:

Ernest Hoffman

(507) 284-2302

Hoffman.EMatthew@mayo.edu

More information

Publications

Publications are currently not available