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Enrolling by invitation NCT06805032

Accuracy and Precision of Train-of-Four Ratios Obtained With Acceleromyography and Electromyography in Restricted-Movement Settings in the Absence of Neuromuscular Blocking Drugs

— Observational Cystoscopy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Observation of EMG and AMG readings.
Who it may be relevant to
Registry conditions: Cystoscopy. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The purpose of this research is to compare the performance of acceleromyograph and electromyograph-based quantitative neuromuscular monitors when the arms are tucked for surgical positioning.

Interventions

  • Other Observation of EMG and AMG readings
    Simultaneous readings from electromyograph and acceleromyograph

Primary outcome measures

  • Accuracy and precision [Time frame: 120 minutes]

Eligibility criteria

Inclusion criteria

  • Patients willing to participate and provide an informed consent.
  • Patients undergoing elective surgical procedures that require general anesthesia without use of NMBA agents administered intraoperatively, and tucked arms.
  • Anticipated surgery duration < 120 minutes.

Exclusion criteria

  • Patients with disorders, such as stroke, carpal tunnel syndrome, broken wrist with nerve damage, Dupuytren contracture, or any similar wrist injury.
  • Patients with systemic neuromuscular diseases such as myasthenia gravis.
  • Patients having surgery that would involve prepping the arm into the sterile field.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

United States · 1 center
  • Mayo Clinic — Jacksonville

Identifiers

NCT: NCT06805032 · 24-011159

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗