NMT EasyFit Sensor and Cable

Conditions

• NMT
• Neuromuscular Blockade Monitoring

Eligibility Criteria

Sex

ALL

Age

18 Years - N/A

Healthy Volunteers

Not accepted

Interventions

• 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.

Study Details

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.

Key Dates

First listed

Feb 6, 2026

Start date

Jun 18, 2026

Status verified

Jul 2026

Primary completion

Oct 31, 2026

Completion

Dec 31, 2026

Study Design

Enrollment

30 participants (estimated)

Allocation

NA

Intervention model

SINGLE_GROUP

Primary purpose

DEVICE_FEASIBILITY

Arms

• Experimental: All Subjects
  Placement of NMT Sensor on Hand and Forearm

Primary Outcome Measure

Collection of End User Feedback Surveys [ Time Frame: Up to 24 hours ]

Central Contacts

• Melissa McCabe, MD
  909-558-4475
  [email protected]

Locations (1)

Find similar trials in Loma Linda, CA