NMT EasyFit Sensor and Cable
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorGE Healthcare
About this trial
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 criteria
Qualifiers
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.
Disqualifiers
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.
Trial design
Treatments tested in this trial
- Collection of NMT Technology
Treatment groups
30 Participants
are divided into 1 treatment groupSponsors and collaborators
GE Healthcare
Lead sponsor
Loma Linda University
Collaborator
Source ClinicalTrials.gov