Orotracheal Intubation with the ORION Videolaryngoscope Versus the King Vision Videolaryngoscope in Adult Patients Without Predictors of a Difficult Airway
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 50
- 试验地点
- 2
- 主要终点
- Successful first attempt
研究概览
简要总结
This study aims to compare the ORION video laryngoscope with the King Vision video laryngoscope for orotracheal intubation in patients without predictors of difficult airway scheduled for elective surgery under general anesthesia.
详细描述
The video laryngoscope, compared to direct laryngoscopy, provides better visualization of the laryngeal and glottic structures, a higher success rate for intubation on the first attempt, and a lower incidence of complications such as mucosal injury, dental injury, and esophageal intubations. Despite the advantages offered by video laryngoscopy, its use is not widespread in developing countries due to high costs. For this reason, the ORION video laryngoscope was developed as a low-cost, reusable device that can undergo high-level disinfection. It is designed using additive manufacturing and meets the standards for biocompatibility, rigidity, and resistance. Additionally, it has undergone preclinical testing in simulation models where anesthesiologists have approved its use in real clinical scenarios. In this study, patients scheduled for elective surgery under general anesthesia without predictors of difficult airway will be included and randomized to be intubated with either the ORION video laryngoscope or the King Vision video laryngoscope. The study will compare the success of intubation on the first attempt, the time taken for intubation, the level of visualization of the glottic structures, and the associated complications between the two video laryngoscopes.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Patients over 18 years of age scheduled for elective surgery requiring general anesthesia.
- •Patients without predictors of difficult airway.
- •Patients with ASA I-II classification.
- •Patients with BMI less than 35 kg/mts2.
排除标准
- •Pregnant women.
- •Patients requiring emergency surgery.
- •Patients with chronic obstructive pulmonary disease.
- •Patients with a history of chronic ischemic heart disease.
- •Patients with a history of asthma.
- •Patients who have not signed the informed consent to participate in the study.
结局指标
主要结局
Successful first attempt
时间窗: After the endotracheal intubation completed
Measurement of orotracheal intubations obtained in the first attempt of videolaryngoscopy with the two videolaryngoscopes, successful orotracheal intubation will be corroborated by capnography. Measured in percentage (%).
次要结局
- Laryngeal visualisation measured with the POGO scale(After the endotracheal intubation completed)
- Esophageal intubation(After the endotracheal intubation completed)
- Intubation time(After the endotracheal intubation completed)
- Laryngeal visualisation measured with the Cormack Lehane scale(After the endotracheal intubation completed)
- Complications(After the endotracheal intubation completed)
- Number of video laryngoscopy attempts(After the endotracheal intubation completed)
- Intubation failure(After the endotracheal intubation completed)
研究者
Juan Fernando Bautista Garcia
M.D.
Hospital General de México Dr. Eduardo Liceaga
