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Clinical Trials/NCT02575443
NCT02575443
Completed
Not Applicable

Neuromuscular Block and Anesthetic Depth Monitoring

Seoul National University Bundang Hospital1 site in 1 country60 target enrollmentSeptember 2015

Overview

Phase
Not Applicable
Intervention
Rocuronium (MB group)
Conditions
Cholecystectomy, Laparoscopic
Sponsor
Seoul National University Bundang Hospital
Enrollment
60
Locations
1
Primary Endpoint
Total infused dose of propofol
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The purpose of this study is to evaluated whether the depth of neuromuscular block may affect the unicon value of anesthetic depth monitoring system (ADMS).

Registry
clinicaltrials.gov
Start Date
September 2015
End Date
September 2017
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hyo-Seok Na

Dr

Seoul National University Bundang Hospital

Eligibility Criteria

Inclusion Criteria

  • Gall bladder disease
  • American Society of Anesthesiologist physical status 1 or 2

Exclusion Criteria

  • Pregnancy
  • Body mass index \< 16
  • Body mass index \>30
  • Neuromuscular disease
  • Previous intraabdominal surgery

Arms & Interventions

Moderate block (MB) group

Intervention: Rocuronium (MB group)

Deep block (DB) group

Intervention: Rocuronium (DB group)

Outcomes

Primary Outcomes

Total infused dose of propofol

Time Frame: At 1 min after the anesthesia is finished

Secondary Outcomes

  • Electromyographic index presented on the anesthetic depth monitoring system(Through study completion, an average of 2 hours)

Study Sites (1)

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