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临床试验/NCT06474559
NCT06474559招募中不适用

Comparison of Protector Laryngeal Mask With Endotracheal Tube: Evaluation of Respiratory Mechanical Parameters During Controlled Ventilation & Possibility of Pulmonary Aspiration

University Hospital of Patras2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
80
试验地点
2
主要终点
Difference in PIP cmH20 (Peak inspiratory pressure ) between the two groups of patients.

研究概览

简要总结

The aim of this prospective, randomized, comparative, controlled clinical study is to compare laryngeal mask airway ProtectorTM with the endotracheal tube, regarding to the respiratory mechanical parameters during controlled mechanical ventilation and the prevalence of aspiration. Aspiration will be evaluated by detecting and quantifying pepsin (a marker of gastric aspiration) and α-amylase (a marker of salivary aspiration) in the bronchoalveolar lavage ( mini BAL) of patients ≥18 years old, ASA 1-2, undergoing selective low-risk surgery under general anesthesia in a lithotomy position.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
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

入选标准

  • Patients aged ≥18 years ASA1-2 who are to undergo planned urological surgery of low or intermediate severity, under general anesthesia in the lithotomy position.

排除标准

  • patients < 18 years old.
  • Patients who are going to undergo an emergency/urgent operation/ trauma patients.
  • Maternal population.
  • Patients who are not scheduled to receive general anesthesia, but some other type of anesthesia.
  • Patients in whom LMA placement is contraindicated, such as patients at high risk for reflux and aspiration of gastric contents (eg, history of gastroesophageal reflux, hiatal hernia, pyloric stenosis, gastrointestinal obstruction, morbid obesity).
  • Patients who meet at least one of the four RODS difficulty criteria.
  • Contraindicated patients: administration of neuromuscular blockade, suppression of spontaneous respiration, and those with an indication for awake intubation or surgical airway.
  • Patients who refuse to participate in the study.

结局指标

主要结局

Difference in PIP cmH20 (Peak inspiratory pressure ) between the two groups of patients.

时间窗: Intraoperative

Measured by Ventilator

Assessment of aspiration risk by quantitative measurements of pepsin (ng/ml) and α-amylase (IU/ml) in BAL of patients and differences in its incidence between the two groups.

时间窗: through study completion, an average of 1 year

Measured by ELISA method

次要结局

  • Differences in lung mechanics between the two patient groups(Intraoperative)

研究者

发起方
University Hospital of Patras
申办方类型
Other
责任方
Principal Investigator
主要研究者

Stella Antoniou

MD

University Hospital of Patras

研究点 (2)

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