Comparing Train-of-Four Recovery in the Adductor Pollicis Versus the Adductor Digiti Minimi in Elective Surgery Patients

NCT ID: NCT06467448

Last Updated: 2026-01-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

57 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-03-18

Study Completion Date

2025-06-01

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Anesthesia Neuromuscular Blockade

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Adductor Pollicis EMG

The Train of Four Ratio will be recorded at 90% as a time and as a reference point

EMG Assessement of Recovery of Neuromuscular Function

Intervention Type DEVICE

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%

EMG Assessement of Recovery of Neuromuscular Function

Intervention Type DEVICE

EMG Train of Four Assessment of Recovery of Neuromuscular Function

Interventions

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EMG Assessement of Recovery of Neuromuscular Function

EMG Train of Four Assessment of Recovery of Neuromuscular Function

Intervention Type DEVICE

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of North Carolina, Chapel Hill

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Stuart Grant

Role: PRINCIPAL_INVESTIGATOR

University of North Carolina, Chapel Hill

Locations

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University of North Carolina at Chapel Hill

Chapel Hill, North Carolina, United States

Site Status

Countries

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United States

Other Identifiers

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24-1013

Identifier Type: -

Identifier Source: org_study_id

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