NMT EasyFit Sensor and Cable
Evaluate Functionality and Use of the NMT EasyFit Sensor and NMT EasyFit Cable
GE Healthcare
30 participants
Jun 18, 2026
INTERVENTIONAL
Conditions
Summary
The purpose of this clinical study is to collect and assess feedback from clinical users regarding the functionality and device use and collection of raw parameter date from the NMT Sensor and NMT Cable.
Eligibility
Inclusion Criteria4
- Study subject (male or female) is age 18 years or older (≥18 years).
- Study subject must have the ability to understand and provide written informed consent.
- Study subject is undergoing a clinically indicated procedure requiring the use of paralytic medication.
- Study subject will have the primary NMT monitoring conducted using an NMT ElectroSensor on the hand/forearm.
Exclusion Criteria8
- Are known to be pregnant.
- Are breastfeeding.
- Suffering from an infection(s) that requires isolation.
- Deformity, scar tissue, tattoos, or other characteristics at the sensor application area that could interfere (e.g., nerve damage) with the completion of the study procedure or identify a study subject.
- Subjects requiring rapid sequence induction
- Subjects expected to be at risk from participation for any reason, such as those with known allergy or sensitivity to adhesive materials that may be used in the study.
- Direct employees or contractors of GE HealthCare, or any company that makes NMT monitoring devices (sensors, cables, modules).
- NMT ElectroSensor placed on the foot/ankle
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Interventions
Collection and assessment of non-invasive electrical stimuli from the NMT measurement placed on the patient's hand and forearm to measure the level of neuromuscular blocking agents during standard of care surgical procedures.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07394140