Clinical Trial

Peripheral Regional Blockade and EMG

Study acronym: Electromyogram
Enrolling by Invitation
View on ClinicalTrials.gov →
Summary
The investigators are studying a type of technology that is already used called surface electromyography (EMG). This measures and records electrical activity using sensor stickers in a non-invasive way. The purpose of this study is to use a prototype/test surface EMG machine to measure how well regional anesthesia (nerve block) is working. This device is non-invasive and being used for research use as an unapproved medical device. The information may teach us how to give nerve blocks more safely and effectively. Study participation: Subjects having surgery will have the surface EMG sensor stickers placed on their arms or legs before surgery. These will stay on during surgery and for part of recovery. Study visits: The study will consist of 1 visit that starts in the pre-operative area, through the surgery, and for part of recovery time after surgery.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-05-13; most recent amendment 2025-10-29.
Status change: Not Yet Recruiting → Enrolling by Invitation 2025-08-19
Trial Details
NCT Number NCT06982027
Lead Sponsor Nationwide Children's Hospital
Conditions Surgery
Enrollment 100 participants
Start Date 2025-09-03
Primary Completion 2027-01 (estimated)
Study Completion 2027-12 (estimated)
Updated on ClinicalTrials.gov 2025-10-30