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Clinical Trial Summary

Compare the reversal effect of neostigmine and sugammadex using quantitative neuromuscular monitoring


Clinical Trial Description

At the end of surgery, decide the dosage of reversal referring to quantitative neuromuscular monitoring value (TOF). After the administration of reversal, the anesthesiologist who are going to manage the participant should not check the quantitative neuromuscular monitoring and determine the timing of extubation only with his (or her) judgement. After entering post-anaesthesia care unit (PACU) measure the TOF value and check the incidence of TOF ratio > 0.9 between the neostigmine group and sugammadex group. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03292965
Study type Interventional
Source Seoul National University Bundang Hospital
Contact
Status Completed
Phase N/A
Start date September 28, 2017
Completion date November 29, 2017

See also
  Status Clinical Trial Phase
Not yet recruiting NCT05053594 - Different Doses of Neostigmine for Reversal of Moderate Neuromuscular Blockade in Children Phase 4
Completed NCT03831815 - Evaluation of Residual Neuromuscular Blockade and of Late Recurarization in the Post Anesthesia Care Unit in Patients Undergoing Videolaparoscopic Cholecystectomy
Recruiting NCT05724550 - Diaphragm Function After Reversal of Rocuronium-induced Neuromuscular Blockade With Sugammadex or Neostigmine in Children N/A