Measuring the electromyographic (EMC) muscle response
Recruiting
- Conditions
- patients receiving neuromuscular blocking agents required for their clinical care during a surgical procedure
- Registration Number
- NL-OMON23335
- Lead Sponsor
- university medical center groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
Age 18 years or older;
- Subject meets the American Society of Anesthesiology (ASA) physical status
I-III criteria (Table I);
Exclusion Criteria
- Presence of an underlying neuromuscular disease
- Presence of renal or hepatic disease
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary objective of this study is to provide EMG performance data of the TetraGraph device on anesthetized subjects. Performance will be assessed post hoc by analyzing objective EMG data and correlating with the responses to annotations made during the surgical procedure (e.g., correlating the EMG responses to the time of NMBA administration).
- Secondary Outcome Measures
Name Time Method o Investigating the quality of the applied skin electrodes (clinically available 3M Red Dot electrodes)<br><br /><br /><br>o Observing the applicability of the prototype (easy of use, …)<br>