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

ConditionUnrecognized Condition

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age18+

SponsorQueen Savang Vadhana Memorial Hospital, Thailand

About this trial

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

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients in emergency department that have indication for conventional intubation

Age > 18 yr

Disqualifiers

Patient who undergo RSI

Patient who falls in cardiac arrest airway algorithm

Patient who is currently pregnancy

Known allergy to lidocaine

Trial design

Design model

Single group

Treatments tested in this trial

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

Treatment groups

110 Participants

are divided into 2 treatment groups

Group A: Lidocaine sprayActive comparator 1 intervention

Group B: PlaceboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

First-pass success rate

Comparison of the succession rate of endotracheal tube intubation

Time frame

1 Year

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Queen Savang Vadhana Memorial Hospital, Thailand

Lead sponsor

Source ClinicalTrials.gov

Apply now