Dose Finding Study of Remimazolam for Laryngeal Mask Airway Insertion

Last updated: March 16, 2022
Sponsor: Yonsei University
Overall Status: Active - Recruiting

Phase

N/A

Condition

Orthopedic Surgery

Orthopedics

Treatment

N/A

Clinical Study ID

NCT05298228
4-2021-1706
  • Ages 19-65
  • All Genders

Study Summary

Laryngeal mask airways (LMA) are widely used in patients receiving general anesthesia and are known to have the following advantages over the endotracheal tube: lower incidence of postoperative sore throat, lower incidence of cough during emergence, and lower incidence of postoperative vomiting. Although LMAs can be inserted without the use of muscle relaxants, a sufficient depth of anesthesia is necessary for placement. Remimazolam is a newer anesthetic that is ultra-short acting with a rapid onset and short context-sensitive half-life allowing for fast recovery. However, the dose of remimazolam needed for LMA insertion without muscle relaxants is not well known. This dose-finding study aims to find the ED50 and ED95 of a single bolus dose of remimazolam for LMA insertion without muscle relaxants in adult patients.

This is an interventional study done in a single group using the Dixon's up-and-down method which requires at least six success/failure pairs in the same direction. The primary endpoint of this study is to investigate the dose of remimazolam associated with 50% (ED50) and 95% (ED95) probability for adequate depth of anesthesia for LMA insertion without muscle relaxants. The beginning dose of remimazolam is 0.3 mg/kg, and when LMA insertion is successful, the dose will be decreased by 0.05 mg/kg in the next patient. When LMA insertion is unsuccessful (failed), the dose will be increased by 0.05 mg/kg in the next patient. Successful LMA insertion is defined as symmetrical chest wall movement and square-wave capnographic traces observed with manual ventilation.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Adult patients aged 19~65 year
  • ASA class I~III
  • Patients scheduled for orthopedic surgery under general anesthesia and eligible forLMA use.

Exclusion

Exclusion Criteria:

  • Patient refusal
  • Patients unable to read consent form
  • Anticipated difficult mask ventilation
  • Active URI or uncontrolled asthma
  • Pneumonia
  • Risk of aspiration such as GERD
  • History of allergies to benzodiazepines
  • Decreased liver or kidney function
  • Pregnant or breastfeeding patients
  • BMI > 30kg/m2
  • History of substance abuse/addiction

Study Design

Total Participants: 25
Study Start date:
March 01, 2022
Estimated Completion Date:
July 27, 2023

Connect with a study center

  • Yonsei University Health System, Severance Hospital

    Seoul,
    Korea, Republic of

    Active - Recruiting

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