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Clinical Trials/NL-OMON42193
NL-OMON42193
Completed
Not Applicable

An International Multi-Center Cohort Study of the Incidence of Anesthesia Awareness Following Laryngoscopy and Intubation - Intraoperative Anaesthesia Awareness Following Induction of Anaesthesia

anesthesiologie- onderzoeksbureau0 sites25 target enrollmentTBD
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ConditionsanesthesieIntraoperative AwarenessIntraoperative Complications

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
anesthesie
Sponsor
anesthesiologie- onderzoeksbureau
Enrollment
25
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
anesthesiologie- onderzoeksbureau

Eligibility Criteria

Inclusion Criteria

  • •1\. Age \>\= 18 years old
  • •2\. English competent
  • •3\. Informed consent obtained
  • •4\. Patients clinically requiring general anesthesia and intubation
  • •5\. Only patients able to safely follow the IFT commands when awake and prior to their operation, per discretion of the PI.

Exclusion Criteria

  • •1\. Age \< 18 years old
  • •2\. Unable or unwilling to sign consent
  • •3\. Unable to undergo postoperative questions
  • •4\. Contraindication to IFT test such as unable to have tourniquet on arm for the IFT (e.g. lymphedema or operative site), rapid sequence inductions and requiring paralysis for laryngoscopy and intubation, per discretion of the PI.

Outcomes

Primary Outcomes

Not specified

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