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Clinical Trials/JPRN-jRCT1032210192
JPRN-jRCT1032210192
Completed
Phase 3

Comparison between a conventional method and the use of an automated cuff pressure controller device in the effective sealing pressure: a randomized controlled study.

Okuda Yasuhisa0 sites70 target enrollmentJuly 9, 2021
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Conditionselective cases under general anesthesiaThe cuff pressure of endotracheal tube

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
elective cases under general anesthesia
Sponsor
Okuda Yasuhisa
Enrollment
70
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 9, 2021
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Okuda Yasuhisa

Eligibility Criteria

Inclusion Criteria

  • •1\) Patients scheduled to undergo tracheal intubation for general anesthesia surgery
  • •2\) Patients with a preoperative ASA Physical Classification System (Class I or II).
  • •Class I: No organic, physiological, biochemical, or psychological abnormalities. The disease to be operated on is localized and does not cause systemic (systematic) damage. The disease to be operated on is localized and does not cause systemic (systematic) damage.
  • •Class II Mild to moderate systematic disorder. The causes are
  • •The cause of the disorder is a disease that has been the subject of surgical treatment, or a condition other than the above, or a physiological cause. Physiological causes.
  • •3\) Patients who can give written consent to participate in this study and who are 20 years of age or older at the time of consent.

Exclusion Criteria

  • •1\) Patients undergoing emergency surgery
  • •2\) Patients who need to be repositioned
  • •3\) Patients who are expected to have difficulty in intubation

Outcomes

Primary Outcomes

Not specified

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