Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06661967

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

Led by Queen Savang Vadhana Memorial Hospital, Thailand · Updated on 2024-10-28

110

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients in emergency department that have indication for conventional intubation
  • Age > 18 yr
Not Eligible

You will not qualify if you...

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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Queen Savang Vadhana Memorial Hospital

Chon Buri, Changwat Chon Buri, Thailand, 20110

Actively Recruiting

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Research Team

S

Sila Thammongkol

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

2

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