Topical Oral Anesthesia Adjuncts in Conventional Intubation on First-Pass Success Rate
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Lidocaine spray.
- Who it may be relevant to
- Registry conditions: Unrecognized Condition. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Thailand
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Topical Oral Anesthesia Adjuncts in Conventional Intubation: A Randomized Controlled Trial Evaluating the Impact of Topical Oral Anesthesia on First-pass Success Rate
Overview
This study aims to determine the first-pass success rate in video laryngoscopy and other parameters that topical anesthesia can affect during intubation.
Detailed description
In Thailand, conventional intubation or sedation without paralysis is still the most common method of intubation due to the lack of emergency physicians at primary care centers. A pilot study had shown that topical oral anesthesia can improve the first-pass success rate in conventional intubation by direct laryngoscopy. This study aims to determine the first-pass success rate in video laryngoscopy and other parameters that topical anesthesia can affect during intubation.
Interventions
- Drug Lidocaine spray
Comparison of the success rate of endotracheal intubations between lidocaine spray and placebo
Primary outcome measures
- First-pass success rate [Time frame: 1 Year]
Eligibility criteria
Inclusion criteria
- Patients in emergency department that have indication for conventional intubation
- Age > 18 yr
Exclusion criteria
- Patient who undergo RSI
- Patient who falls in cardiac arrest airway algorithm
- Patient who is currently pregnancy
- Known allergy to lidocaine
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Single group
- Masking
- Triple blind
- Primary purpose
- Treatment
Study locations
Thailand · 1 center
- Queen Savang Vadhana Memorial Hospital — Chon Buri
Identifiers
NCT: NCT06661967 · 017/2567