Queen Savang Vadhana Memorial Hospital
Chon Buri, Changwat Chon Buri, 20110, Thailand
Location status: Recruiting
NCT Number: NCT06661967
This study aims to determine the first-pass success rate in video laryngoscopy and other parameters that topical anesthesia can affect during intubation.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Chon Buri, Changwat Chon Buri, 20110, Thailand
Location status: Recruiting
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Comparison of the success rate of endotracheal intubations between lidocaine spray and placebo
Other names: Placebo
Time frame: 1 Year
Comparison of the succession rate of endotracheal tube intubation
Contact information is provided by the study sponsor or research team.
Queen Savang Vadhana Memorial Hospital, Thailand
Other
Topical Oral Anesthesia Adjuncts in Conventional Intubation: A Randomized Controlled Trial Evaluating the Impact of Topical Oral Anesthesia on First-pass Success Rate
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05319132
Unrecognized Condition
Lyon, Auvergne-Rhône-Alpes, France
View Trial DetailsNCT06803199
Unrecognized Condition
Kaohsiung City, Taiwan
View Trial DetailsNCT06243146
Unrecognized Condition
Chengdu, Sichuan, China
View Trial DetailsNCT06546774
Genital Diseases, Infertility
Kaohsiung City, Taiwan
View Trial Details