跳至主要内容
临床试验/NCT07249983
NCT07249983招募中不适用

Evaluation of SaCoVLM™ Video Laryngeal Mask Airway for Airway Management by Inexperienced Military Medics: A Two-Phase Feasibility Study

Charles University, Czech Republic1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2026年3月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
50
试验地点
1
主要终点
First-Attempt Success Rate of SaCoVLM™ Insertion

研究概览

简要总结

A prospective, two-phase interventional study evaluating the performance, safety, and usability of the SaCoVLM™ video laryngeal mask airway for airway management by military medics with limited intubation experience. The study includes simulation-based training and clinical application in sedated patients undergoing elective surgery.

详细描述

This prospective, two-phase study evaluates the use of the SaCoVLM™ video laryngeal mask airway by military medics with limited airway experience. Phase 1 involves simulated intubation on manikins to assess device placement, visualization quality, and intubation success. Phase 2 evaluates clinical performance in adult patients undergoing elective surgery under general anesthesia. Key outcomes include first-attempt success rates, insertion and intubation times, glottic visualization scores, and complication rates. The study aims to determine whether SaCoVLM™ can enable safe and effective airway management in resource-limited and prehospital military settings.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Elective surgery
  • need for airway management

排除标准

  • Pregnancy
  • known airway abnormalities
  • allergy to anesthetics

研究组 & 干预措施

Simulation and Clinical Phase

Experimental

Simulation-based and clinical use of SaCoVLM™ for airway management and intubation.

干预措施: SaCoVLM™ Video Laryngeal Mask (Device)

结局指标

主要结局

First-Attempt Success Rate of SaCoVLM™ Insertion

时间窗: Within 10 minutes of airway intervention.

Proportion of cases in which the SaCoVLM™ is successfully inserted on the first attempt during both simulated and clinical phases.

First-Attempt Success Rate of Orotracheal Intubation via SaCoVLM™

时间窗: Within 10 minutes following SaCoVLM™ placement.

Proportion of successful orotracheal intubations on the first attempt using the SaCoVLM™ device as a conduit.

次要结局

  • Time to SaCoVLM™ Insertion(During initial airway management (simulation or clinical setting).)
  • Time to Successful Intubation(During initial airway management (simulation or clinical setting).)
  • Glottic Visualization Score(Immediately after SaCoVLM™ placement.)
  • Subjective Difficulty Score(Immediately after each procedure.)
  • Incidence of Airway Complications(From initiation of airway management to induction of general anesthesia (clinical phase only).)

研究者

发起方
Charles University, Czech Republic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Michal Soták

Principal Investigator

Charles University, Czech Republic

研究点 (1)

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