RecruitingNot ApplicableNCT06661967

Topical Oral Anesthesia Adjuncts in Conventional Intubation on First-Pass Success Rate

Topical Oral Anesthesia Adjuncts in Conventional Intubation: A Randomized Controlled Trial Evaluating the Impact of Topical Oral Anesthesia on First-pass Success Rate


Sponsor

Queen Savang Vadhana Memorial Hospital, Thailand

Enrollment

110 participants

Start Date

Oct 25, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to determine the first-pass success rate in video laryngoscopy and other parameters that topical anesthesia can affect during intubation.


Eligibility

Min Age: 18 Years

Inclusion Criteria2

  • Patients in emergency department that have indication for conventional intubation
  • Age > 18 yr

Exclusion Criteria4

  • Patient who undergo RSI
  • Patient who falls in cardiac arrest airway algorithm
  • Patient who is currently pregnancy
  • Known allergy to lidocaine

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGLidocaine spray

Comparison of the success rate of endotracheal intubations between lidocaine spray and placebo


Locations(1)

Queen Savang Vadhana Memorial Hospital

Chon Buri, Changwat Chon Buri, Thailand

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06661967


Related Trials