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Clinical Trials/NCT02657187
NCT02657187
Unknown
Not Applicable

The Neuromuscular Effect of Rocuronium in Patient Measuring Muscle Mass by Bioelectrical Impedance Analysis

Go Eun Bae1 site in 1 country80 target enrollmentFebruary 2016
ConditionsAnesthesia
InterventionsInbodyRocuronium

Overview

Phase
Not Applicable
Intervention
Inbody
Conditions
Anesthesia
Sponsor
Go Eun Bae
Enrollment
80
Locations
1
Primary Endpoint
percentage of neuromuscular block
Last Updated
10 years ago

Overview

Brief Summary

Rocuronium block neuromuscular transmission at the neuromuscular junction, causing paralysis of the affected skeletal muscles. There have been several studies reported positive relationship between muscle mass and amount of neuromuscular junction. The purpose of this study is to find 50% effective dose and 95% effective dose of rocuronium according to muscle mass.

Detailed Description

Rocuronium block neuromuscular transmission at the neuromuscular junction, causing paralysis of the affected skeletal muscles. There have been several studies reported positive relationship between muscle mass and amount of neuromuscular junction. Until now, dose of rocuronium has been judged by patient's weight and height. When the rocuronium was developed, 50% effective dose and 95% effective dose of rocuronium was calculated by patient corrected body weight which used weight and height. However, height and weight do not represent exact muscle mass. The purpose of this study is to find 50% effective dose and 95% effective dose of rocuronium according to muscle mass. Measurement of muscle mass will be obtained using bioelectrical impedence analysis.

Registry
clinicaltrials.gov
Start Date
February 2016
End Date
August 2016
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Go Eun Bae
Responsible Party
Sponsor Investigator
Principal Investigator

Go Eun Bae

Clinical instructor

Korea University Anam Hospital

Eligibility Criteria

Inclusion Criteria

  • All patient who undergo general anesthesia

Exclusion Criteria

  • Liver and kidney disease
  • Any types of muscle disorder.
  • Metal materials or pacemaker in body

Arms & Interventions

rocuronium 1

Participant measure muscle mass by bioelectrical impedance analysis (Inbody 720, Inbody, Seoul, Korea) and the dose of rocuronium is 0.24mg per muscle mass(kg).

Intervention: Inbody

rocuronium 1

Participant measure muscle mass by bioelectrical impedance analysis (Inbody 720, Inbody, Seoul, Korea) and the dose of rocuronium is 0.24mg per muscle mass(kg).

Intervention: Rocuronium

rocuronium 2

Participant measure muscle mass by bioelectrical impedance analysis (Inbody 720, Inbody, Seoul, Korea) and the dose of rocuronium is 0.32mg per muscle mass(kg).

Intervention: Inbody

rocuronium 2

Participant measure muscle mass by bioelectrical impedance analysis (Inbody 720, Inbody, Seoul, Korea) and the dose of rocuronium is 0.32mg per muscle mass(kg).

Intervention: Rocuronium

rocuronium 3

Participant measure muscle mass by bioelectrical impedance analysis (Inbody 720, Inbody, Seoul, Korea) and the dose of rocuronium is 0.40mg per muscle mass(kg).

Intervention: Inbody

rocuronium 3

Participant measure muscle mass by bioelectrical impedance analysis (Inbody 720, Inbody, Seoul, Korea) and the dose of rocuronium is 0.40mg per muscle mass(kg).

Intervention: Rocuronium

rocuronium 4

Participant measure muscle mass by bioelectrical impedance analysis (Inbody 720, Inbody, Seoul, Korea) and the dose of rocuronium is 0.48mg per muscle mass(kg).

Intervention: Inbody

rocuronium 4

Participant measure muscle mass by bioelectrical impedance analysis (Inbody 720, Inbody, Seoul, Korea) and the dose of rocuronium is 0.48mg per muscle mass(kg).

Intervention: Rocuronium

Outcomes

Primary Outcomes

percentage of neuromuscular block

Time Frame: ten minutes

percentage of neuromuscular block is calculated by ratio of T1 to T4. T1 is result of first stimulation and T4 is result of fourth stimulation which are obtained by commonly used neuromuscular monitoring device.

Secondary Outcomes

  • onset time(ten minutes)

Study Sites (1)

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