Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07394140

NMT EasyFit Sensor and Cable

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.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Loma Linda University Health

Loma Linda, California, 92354, United States

Location status: Recruiting

Location contact

Melissa McCabe

CONTACT

[email protected]

909-558-4256

Melissa McCabe, MD

PRINCIPAL_INVESTIGATOR

About this study

The NMT Sensor provides quantitative, automated measurements of neuromuscular block by delivering non-invasive electrical stimuli to the ulnar nerve and recording electromyography (EMG) responses from the adductor pollicis muscle. Surface hydrogel electrodes with adhesive foam ensure secure placement for continuous monitoring. The single-use sensor connects to a reusable NMT Cable and is designed for use with GE HealthCare NMT measurement devices (NMT Module and bedside monitors).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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 criteria

  • 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

Treatment and study plan

Collection of NMT Technology

Device

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.

Primary outcomes

  1. Collection of End User Feedback Surveys

    Time frame: Up to 24 hours

    Collection of end user feedback surveys on the functionality and clinical use of the NMT Sensor and Cable during standard of care surgical procedure (minimum of 1 hour and maximum of 24 hours).

Secondary outcomes

  1. Collection of raw parameter data from NMT Sensor and Cable

    Time frame: Up to 24 hours

    Collection of raw parameter data from NMT Sensor and Cable to evaluate the reliability of the measurements to NMBA concordance rate.

  2. Incidence of Safety Events

    Time frame: 4 months.

    Analysis of adverse events will be listed per subject, summarized with counts and percentages of events, and summarized with counts and percentages of subjects with events.

Study contacts

Contact information is provided by the study sponsor or research team.

Melissa McCabe, MD

CONTACT

[email protected]

909-558-4475

Sponsors and collaborators

Lead sponsor

GE Healthcare

Industry

Collaborators

  • Loma Linda University

Registry information

Official study title

Evaluate Functionality and Use of the NMT EasyFit Sensor and NMT EasyFit Cable

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Feb 6, 2026
Registry last updated
Jul 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.