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Clinical Trials/ChiCTR-TRC-14004588
ChiCTR-TRC-14004588
Completed
Not Applicable

Proseal 喉罩与 Supreme 喉罩用于全麻患者气道管理的对比研究:新方法 vs 新喉罩

自筹1 site in 1 country120 target enrollmentStarted: May 1, 2014Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
自筹
Enrollment
120
Locations
1
Primary Endpoint
喉罩首次置入成功率

Overview

Brief Summary

评估新置入法用于全麻患者 Proseal 喉罩置入的有效性和安全性,并与传统方法以及 Supreme 喉罩相比较。

Study Design

Study Type
干预性研究
Primary Purpose
随机平行对照

Eligibility Criteria

Ages
18 to 86 (—)
Sex
All

Inclusion Criteria

  • 择期行腹腔镜胆囊切除手术患者,年龄≥18 岁,美国麻醉医师协会分级法(ASA)I~Ⅲ,无严重心肺疾病。无困难气道

Exclusion Criteria

  • 年龄<18 岁,ASAⅣ~Ⅴ,体重指数(BMI)>35kg/m2,术前有咽喉疼痛,有严重胃食管反流症,预估困难气道(张口度<2.5cm,Mallampati 4 级)。

Arms & Interventions

Proseal 喉罩组

使用徒手法置入 Proseal 喉罩

Proseal 喉罩改良组

使用导芯塑形法置入 Proseal 喉罩

Outcomes

Primary Outcomes

喉罩首次置入成功率

喉罩置入时间

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
自筹

Study Sites (1)

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