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Clinical Trials/JPRN-jRCT1031210554
JPRN-jRCT1031210554
Recruiting
未知

A study on the efficacy of the loss of response to jaw thrust as a clinical test to assess adequate depth of anesthesia using remimazolam besylate and the dose required for the loss of response.

Okuda Yasuhisa0 sites70 target enrollmentJanuary 17, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Okuda Yasuhisa
Enrollment
70
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 17, 2022
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Okuda Yasuhisa

Eligibility Criteria

Inclusion Criteria

  • 1\) Patients with written consent to participate in this study.
  • 2\) Patients aged between 20 and 65 at the time of consent.
  • 3\) American Society of Anesthesiologists (ASA) Grade I or II patients.
  • 4\) Patients whose surgical purpose is other than heart surgery.

Exclusion Criteria

  • 1\) Patients undergoing emergency surgery.
  • 2\) Patients who may be pregnant.
  • 3\) Patients who are expected to have difficulty airway management or intubation.
  • 4\) BMI 28 and above.
  • 5\) Patients who have high risk of aspiration.
  • 6\) Patients with liver dysfunction: Child\-pugh classification B or higher.
  • 7\) Patients with contraindications to propofol or remimazolam.
  • 8\) Patients with a history of alcoholism or drug abuse.
  • 9\) Patients who regularly use sedatives.
  • 10\) Patients with a history of cervical spine / cervical cord disease.

Outcomes

Primary Outcomes

Not specified

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