Purpose

The train-of-four (TOF) ratio is a quantitative measure used in anesthesia to assess the degree of neuromuscular blockade induced by neuromuscular blocking agents during surgical procedures. Current American Society of Anesthesiologists guidelines recommend monitoring the TOF ratio to guide the administration and reversal of NMBAs, with a target ratio of 0.9 or higher at adductor pollicis muscle indicating adequate reversal and restoration of neuromuscular function. This proposed study aims to observe and compare the TOF ratio between two different muscles of the hand: adductor pollicis and adductor digiti minim using anesthesia monitors on both of their arms during recovery of neuromuscular function. Surgery and anesthesia will occur per standard of care.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Surgery and general anesthesia with administration of non depolarizing neuromuscular blocking drug

Exclusion Criteria

  • neuromuscular disease or weakness of one of upper limbs. - Inability to use one of subjects arms to record neuromuscular monitor. - Contraindication to administration or allergy to non depolarizing neuromuscular blocking drug.

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Adductor Pollicis EMG The Train of Four Ratio will be recorded at 90% as a time and as a reference point
  • Device: EMG Assessement of Recovery of Neuromuscular Function
    EMG Train of Four Assessment of Recovery of Neuromuscular Function
Adductor Digiti Minimi The Train of Four Ratio will be recorded when the adductor pollicis ratio reads 90%
  • Device: EMG Assessement of Recovery of Neuromuscular Function
    EMG Train of Four Assessment of Recovery of Neuromuscular Function

Recruiting Locations

University of North Carolina at Chapel Hill
Chapel Hill, North Carolina 27599
Contact:
Stuart Grant, MB ChB
919-966-5136
stuart_grant@med.unc.edu

More Details

NCT ID
NCT06467448
Status
Recruiting
Sponsor
University of North Carolina, Chapel Hill

Study Contact

Stuart A Grant, MB ChB
9194456732
stuart_grant@med.unc.edu

Detailed Description

The study population will enroll adult patients (>18) who will receive non-depolarizing neuromuscular blocking drugs as part of a routine general anesthetic and who will have monitoring of their recovery from neuromuscular block performed using the Tetragraph (Senzime Sweden). Patients with upper limb weakness, neurological deficits, and inability to use the other arm to record the second EMG recording will be excluded. Procedures (methods): Adult patients undergoing general anesthesia with the use of muscle relaxants will have anesthesia monitors on both of their arms. On one arm, the study sticky pad will be placed on the forearm and over the base of the little finger. On the other arm, the standard monitor is placed on the forearm and over the base of the thumb. To identify pre-operative patients, an EPIC report will be utilized to screen for eligible participants. Patients will be contacted via phone by a research team member the day before their procedure and enrolled. Informed consent will be formally obtained on the day of the procedure.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.