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Clinical Trials/ChiCTR-IOR-17013089
ChiCTR-IOR-17013089Active, not recruitingNot Applicable

魏氏鼻咽喷射通气道用于无痛胃肠镜的有效性和安全性的研究

经费自筹1 site in 1 country80 target enrollmentStarted: November 1, 2017Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Enrollment
80
Locations
1
Primary Endpoint
最低血氧饱和度

Study Overview

Brief Summary

该研究旨在观察魏氏鼻咽喷射通气道用于无痛胃肠镜的有效性和安全性

Study Design

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

Eligibility Criteria

Ages
18 to 65 (—)
Sex
All

Inclusion Criteria

  • 首都医科大学附属北京友谊医院接受静脉麻醉下无痛胃肠镜患者

Exclusion Criteria

  • ASAIII-IV 级;凝血功能障碍和出血倾向的病人;心脏病患者(如心力衰竭,心绞痛,心肌梗塞,心律失常等);肺部疾病(如哮喘,COPD,肺栓塞,肺水肿等);妊娠;肝功能衰竭;肾功能衰竭;颅内压增高;急诊手术的病人;饱胃病人;多发创伤的病人

Arms & Interventions

魏氏鼻咽通气道组

魏氏鼻咽通气道

鼻氧管组

鼻氧管

Outcomes

Primary Outcomes

最低血氧饱和度

辅助通气次数

鼻出血

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
经费自筹

Study Sites (1)

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