Reversal of Residual Neuromuscular Blockade at Train-of-four Ratio 0.3 With Sugammadex and Neostigmine

Sponsor
Guangzhou General Hospital of Guangzhou Military Command (Other)
Overall Status
Completed
CT.gov ID
NCT03656614
Collaborator
(none)
121
1
11.1
10.9

Study Details

Study Description

Brief Summary

The aim of this study is to estimate the optimal dose of sugammadex and neostigmine reversal of a vecuronium-induced residual neuromuscular block at train-of-four ratio 0.3.

Condition or Disease Intervention/Treatment Phase

Detailed Description

Sugammadex is a modified γ-cyclodextrin compound that reverses the neuromuscular blockade produced by steroidal nondepolarizing muscle relaxants such as rocuronium,vecuronium and pipecuronium by encapsulating them, making them unavailable to interact with the nicotinic acetylcholine receptors at the neuromuscular junction.However, residual neuromuscular blocks between reappearance of T4 and train-of-four ratio (TOFR)=0.5 are more frequent in clinical practice compared with profound or deep blocks and have not been investigated for sugammadex previously.

Unlike neostigmine, sugammadex is efficacious in reversing profound (no responses to either train-of-four (TOF) or posttetanic count stimulation) or deep (posttetanic count of 1 or 2) neuromuscular block (NMB) in doses of 16 and 4 mg/kg, respectively. However, shallow neuromuscular blocks are more frequent in clinical practice compared with profound or deep blocks and have not been investigated for sugammadex previously.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
121 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Dose Finding Study for Reversal of Vecuronium-induced Neuromuscular Blockade at Train-of-four Ratio 0.3 With Sugammadex and Neostigmine
Actual Study Start Date :
Jul 26, 2018
Actual Primary Completion Date :
Jun 28, 2019
Actual Study Completion Date :
Jun 30, 2019

Arms and Interventions

Arm Intervention/Treatment
sugammadex 0.125

Sugammadex group: sugammadex 0.125 mg/kg IV once at the reappearance of TOF 0.3

Drug: Sugammadex
At the end of surgical procedure at a depth of neuromuscular blockade at the reappearance of train-of-four 0.3, single intravenous injection of either : Sugammadex 0.125 mg/kg (sugammadex 0.125) Sugammadex 0.25 mg/kg (sugammadex 0.25) Sugammadex 0.5 mg/kg (sugammadex 0.5) Sugammadex 1.0 mg/kg (sugammadex 1.0) Sugammadex 2.0 mg/kg (sugammadex 2.0)
Other Names:
  • Bridion
  • Org 25969
  • Sugammadex 0.25

    Sugammadex group: sugammadex 0.25 mg/kg IV once at the reappearance of TOF 0.3

    Drug: Sugammadex
    At the end of surgical procedure at a depth of neuromuscular blockade at the reappearance of train-of-four 0.3, single intravenous injection of either : Sugammadex 0.125 mg/kg (sugammadex 0.125) Sugammadex 0.25 mg/kg (sugammadex 0.25) Sugammadex 0.5 mg/kg (sugammadex 0.5) Sugammadex 1.0 mg/kg (sugammadex 1.0) Sugammadex 2.0 mg/kg (sugammadex 2.0)
    Other Names:
  • Bridion
  • Org 25969
  • Sugammadex 0.5

    Sugammadex group: sugammadex 0.5 mg/kg IV once at the reappearance of TOF 0.3

    Drug: Sugammadex
    At the end of surgical procedure at a depth of neuromuscular blockade at the reappearance of train-of-four 0.3, single intravenous injection of either : Sugammadex 0.125 mg/kg (sugammadex 0.125) Sugammadex 0.25 mg/kg (sugammadex 0.25) Sugammadex 0.5 mg/kg (sugammadex 0.5) Sugammadex 1.0 mg/kg (sugammadex 1.0) Sugammadex 2.0 mg/kg (sugammadex 2.0)
    Other Names:
  • Bridion
  • Org 25969
  • Sugammadex 1.0

    Sugammadex group: sugammadex 1.0 mg/kg IV once at the reappearance of TOF 0.3

    Drug: Sugammadex
    At the end of surgical procedure at a depth of neuromuscular blockade at the reappearance of train-of-four 0.3, single intravenous injection of either : Sugammadex 0.125 mg/kg (sugammadex 0.125) Sugammadex 0.25 mg/kg (sugammadex 0.25) Sugammadex 0.5 mg/kg (sugammadex 0.5) Sugammadex 1.0 mg/kg (sugammadex 1.0) Sugammadex 2.0 mg/kg (sugammadex 2.0)
    Other Names:
  • Bridion
  • Org 25969
  • Sugammadex 2.0

    Sugammadex group: sugammadex 2.0 mg/kg IV once at the reappearance of TOF 0.3

    Drug: Sugammadex
    At the end of surgical procedure at a depth of neuromuscular blockade at the reappearance of train-of-four 0.3, single intravenous injection of either : Sugammadex 0.125 mg/kg (sugammadex 0.125) Sugammadex 0.25 mg/kg (sugammadex 0.25) Sugammadex 0.5 mg/kg (sugammadex 0.5) Sugammadex 1.0 mg/kg (sugammadex 1.0) Sugammadex 2.0 mg/kg (sugammadex 2.0)
    Other Names:
  • Bridion
  • Org 25969
  • Neostigmine 10

    Neostigmine group: neostigmine 10 µg/kg IV once at the reappearance of TOF 0.3

    Drug: Neostigmine
    At the end of surgical procedure at a depth of neuromuscular blockade at the reappearance of train-of-four 0.3, single intravenous injection of either : Neostigmine 10 µg/kg (Neostigmine 10) Neostigmine 25 µg/kg (Neostigmine 25) Neostigmine 40 µg/kg (Neostigmine 40) Neostigmine 55 µg/kg (Neostigmine 55) Neostigmine 70 µg/kg (Neostigmine 70) Atropine will be administered with Neostigmine at a half dose of Neostigmine administered through an intravenous line with brisk flow.
    Other Names:
  • Prostigmin
  • Neostigmine 25

    Neostigmine group: neostigmine 25 µg/kg IV once at the reappearance of TOF 0.3

    Drug: Neostigmine
    At the end of surgical procedure at a depth of neuromuscular blockade at the reappearance of train-of-four 0.3, single intravenous injection of either : Neostigmine 10 µg/kg (Neostigmine 10) Neostigmine 25 µg/kg (Neostigmine 25) Neostigmine 40 µg/kg (Neostigmine 40) Neostigmine 55 µg/kg (Neostigmine 55) Neostigmine 70 µg/kg (Neostigmine 70) Atropine will be administered with Neostigmine at a half dose of Neostigmine administered through an intravenous line with brisk flow.
    Other Names:
  • Prostigmin
  • Neostigmine 40

    Neostigmine group: neostigmine 40 µg/kg IV once at the reappearance of TOF 0.3

    Drug: Neostigmine
    At the end of surgical procedure at a depth of neuromuscular blockade at the reappearance of train-of-four 0.3, single intravenous injection of either : Neostigmine 10 µg/kg (Neostigmine 10) Neostigmine 25 µg/kg (Neostigmine 25) Neostigmine 40 µg/kg (Neostigmine 40) Neostigmine 55 µg/kg (Neostigmine 55) Neostigmine 70 µg/kg (Neostigmine 70) Atropine will be administered with Neostigmine at a half dose of Neostigmine administered through an intravenous line with brisk flow.
    Other Names:
  • Prostigmin
  • Neostigmine 55

    Neostigmine group: neostigmine 55 µg/kg IV once at the reappearance of TOF 0.3

    Drug: Neostigmine
    At the end of surgical procedure at a depth of neuromuscular blockade at the reappearance of train-of-four 0.3, single intravenous injection of either : Neostigmine 10 µg/kg (Neostigmine 10) Neostigmine 25 µg/kg (Neostigmine 25) Neostigmine 40 µg/kg (Neostigmine 40) Neostigmine 55 µg/kg (Neostigmine 55) Neostigmine 70 µg/kg (Neostigmine 70) Atropine will be administered with Neostigmine at a half dose of Neostigmine administered through an intravenous line with brisk flow.
    Other Names:
  • Prostigmin
  • Neostigmine 70

    Neostigmine group: neostigmine 70 µg/kg IV once at the reappearance of TOF 0.3

    Drug: Neostigmine
    At the end of surgical procedure at a depth of neuromuscular blockade at the reappearance of train-of-four 0.3, single intravenous injection of either : Neostigmine 10 µg/kg (Neostigmine 10) Neostigmine 25 µg/kg (Neostigmine 25) Neostigmine 40 µg/kg (Neostigmine 40) Neostigmine 55 µg/kg (Neostigmine 55) Neostigmine 70 µg/kg (Neostigmine 70) Atropine will be administered with Neostigmine at a half dose of Neostigmine administered through an intravenous line with brisk flow.
    Other Names:
  • Prostigmin
  • Placebo

    Placebo group: Saline 0.9% IV once at the reappearance of TOF 0.3

    Drug: Saline 0.9%
    At the end of surgical procedure at a depth of neuromuscular blockade at the reappearance of train-of-four 0.3, single intravenous injection of saline 0.9%.
    Other Names:
  • Placebo
  • Outcome Measures

    Primary Outcome Measures

    1. Time to TOF 0.9 after the administration of reversal agent [the general anesthesia time 1 hour at least]

      The time to achieve TOF (Train of Four stimulation) ratio to 0.9 following the investigational drug or placebo administration.

    Secondary Outcome Measures

    1. incidence of reparalysis [approximately 1 hour]

      Determining whether patients receiving reversal agent will have a train-to-four ratio <0.8 during total recovery time (from TOF reach 0.9 first time to post-anaesthesia care unit (PACU) departure)

    2. incidence of adverse event [the general anesthesia and recovery time 2 hours at least]

      Documenting whether patients will have some adverse events(such as hypoxia bradycardia nausea and vomiting) from anesthesia commence to PACU departure.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • 1 age of 18 to 65 yr,

    • 2 body mass index 18.5 to 25.0 kg/m2,

    • 3 American Society of Anesthesiologists physical status I to III

    • 4 scheduled for elective surgery with an expected duration of at least 60min under general anesthesia with intubation of the trachea or laryngeal mask

    • 5 patients having given informed consent to the study

    Exclusion Criteria:
    • 1 patients who had participated in another clinical trial within 1 month

    • 2 Patients with suspected difficult airway, bronchial asthma, chronic obstructive pulmonary disease

    • 3 known neuromuscular disease

    • 4 suspected malignant hyperthermia

    • 5 hepatic or renal dysfunction

    • 6 glaucoma

    • 7 allergy to the medication that used in this trial

    • 8 taking medicaments that might influence the effect of NMB agents

    • 9 pregnant, or breastfeeding state

    • 10 taking medication known to alter the effect of neuromuscular blocking agents( toremifene .etc)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Guangzhou Military Region General Hospital, Department of Anesthesiology Guangzhou Guangdong China 510010

    Sponsors and Collaborators

    • Guangzhou General Hospital of Guangzhou Military Command

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    bo xu, Clinical Professor, Guangzhou General Hospital of Guangzhou Military Command
    ClinicalTrials.gov Identifier:
    NCT03656614
    Other Study ID Numbers:
    • Reversal Neuromuscular Block
    First Posted:
    Sep 4, 2018
    Last Update Posted:
    Aug 11, 2020
    Last Verified:
    Aug 1, 2020
    Keywords provided by bo xu, Clinical Professor, Guangzhou General Hospital of Guangzhou Military Command
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 11, 2020