跳至主要内容
临床试验/NCT07019961
NCT07019961尚未招募不适用

Comparison of the GMA-TULIP and I-gel Laryngeal Mask for Airway Management in General Anaesthesia: a Randomized Controlled Trial

Qilu Hospital of Shandong University1 个研究点 分布在 1 个国家目标入组 198 人开始时间: 2025年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
198
试验地点
1
主要终点
Accuracy of anatomical alignment under fiberoptic bronchoscopy observation

研究概览

简要总结

The goal of this clinical trial is to learn if GMA-TULIP laryngeal mask willfit well in the right place in participants undergoing trauma surgery in a supine position under general anaesthesia.

It will also learn about the convenience, effectiveness and safety of the GMA-TULIP laryngeal mask.

The main questions it aims to answer are:

Does the GMA-TULIP laryngeal mask exhibit better anatomical alignment? Does the GMA-TULIP laryngeal mask perform effectively in trauma surgery patients in a supine position under general anaesthesia? Researchers will compare with the i-gel laryngeal mask (a device already popular among anaesthetists) to see if the GMA-TULIP laryngeal mask works to have a good performance in general anaesthesia.

Participants will describe feelings immediately after anesthesia, 1 hour later and 24 hours later.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •18 years old ≤ age ≤ 70 years old. Patients undergoing trauma surgery in a supine position under general anesthesia.
  • •18 kg/m2 ≤ BMI ≤ 35 kg/m
  • •American Society of Anesthesiologists (ASA) grades I-III. Can understand the research process and the use of pain scales. Clear understanding and voluntary participation in the study, signing of informed consent form.

排除标准

  • •Patients with known or predicted difficult airways. High risk of reflux or aspiration (e.g., gastroesophageal reflux disease patients).
  • •Individuals with active upper respiratory tract infections. Cervical related diseases or surgical history. Preoperative sore throat or previous sore throat or hoarseness. Patients with oral and maxillofacial trauma or fractures. Other reasons why researchers believe it is not appropriate to participate in the experiment.

研究组 & 干预措施

G group

Experimental

Participants who will use the GMA-TULIP laryngeal mask

干预措施: the GMA-TULIP laryngeal mask (Device)

I Group

Active Comparator

Participants who will use the i-gel laryngeal mask

干预措施: the i-gel laryngeal mask (Device)

结局指标

主要结局

Accuracy of anatomical alignment under fiberoptic bronchoscopy observation

时间窗: After insertion of laryngeal mask

Class I: Vocal cords visible. Class II: Vocal cords and posterior epiglottis visible. Class III: Vocal cords and anterior epiglottis visible, \<50% visual obstruction of epiglottis to vocal cords. Class IV: Vocal cords and anterior epiglottis visible, \>50% visual obstruction of epiglottis to vocal cords. Class V: Vocal cords not visible. We define Class I and II field of view as accurate alignment; Class III and IV vision are defined as poor alignment; Class V vision is defined as alignment failure.

次要结局

  • Number of laryngeal mask insertions(After anesthesia induction)
  • Placement time of laryngeal mask(After anesthesia induction)
  • Difficulty level of laryngeal mask insertion(After insertion of laryngeal mask)
  • Time of insertion of gastric tube through laryngeal mask airway(After insertion of laryngeal mask)
  • Number of gastric tube insertions(After insertion of laryngeal mask)
  • Difficulty level of gastric tube insertion(After insertion of laryngeal mask)
  • Oral and pharyngeal leakage pressure(10 minutes after stable ventilation and 1 hour after ventilation)
  • Accuracy of anatomical alignment under fiberoptic bronchoscopy observation(1 hour after ventilation and at the end of surgery)
  • Success rate of initial ventilation placement(During the anesthesia process)
  • Success rate of intraoperative ventilation(During the anesthesia process)
  • Number of laryngeal mask adjustments during surgery(During the anesthesia process)
  • Intraoperative injury situation(During the surgical process)
  • Postoperative respiratory complications(Immediately after anesthesia awakening, 1 hour later, 24 hours later)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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