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临床试验/NCT02495480
NCT02495480Unknown不适用

A Novel Disposable Sheathed Gastroscopic System for Cecal Intubation:Safety and Efficacy in Unsedated Colonoscopies

Yuqi He0 个研究点目标入组 120 人开始时间: 2015年7月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
120
主要终点
Cecal intubation success rate

研究概览

简要总结

A novel disposable sheathed gastroscope system has been shown to be safe and more efficient in clinical practice during gastroscopy. This novel disposable sheathed endoscope system could effectively prevent cross-infection by simply taking off the contaminated sheath after examination of a patient and placing a new sheath on the endoscope. In this way, investigators can save the endoscopic reprocessing time and also decrease the need for endoscopic cleaning and disinfecting equipment.

Participants may think that placing a new sheath on the endoscope can decrease the success rate of cecal intubation in patients undergoing screening colonoscopy. With a new sheath on the endoscope during scope insertion can probably increases distension of the colonic lumen and loop formation. The probable adhesion may increase the discomfort of investigators and participants. But a previous clinical study by investigators' team showed that the participants' feeling were no significant difference (Z = -1.783, P = 0.075) between sheathed and conventional groups. No significant differences were observed in optical clarity, or pathology detection rate. There were no complications, and no microbial contamination was detected. Based on this study, investigators hypothesize that compared with conventional group, placing a new sheath on the endoscope does not significantly reduce the success rate of cecal intubation in average patients.

The aim of the study is to compare the outcome of colonoscopy placing a new sheath on the endoscope versus the conventional method in average participants. The primary outcome is cecal intubation success rate. The secondary outcomes include cecal intubation time, maximum pain score during colonoscopy, overall pain score after colonoscopy and adenoma detection rate.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Screening
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients accepted sedated colonoscopy

排除标准

  • a request for sedation/analgesia at the start of the procedure
  • previous colorectal surgery
  • declining to provide informed consent
  • advanced comorbidity
  • coagulopathy or anticoagulant medication administered
  • failure to comply with the recommended bowel preparation regimen.

结局指标

主要结局

Cecal intubation success rate

时间窗: up to ten months

次要结局

  • Pain according to a 10-point pain scale(up to ten months)

研究者

发起方
Yuqi He
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Yuqi He

Doctor

General Hospital of Beijing PLA Military Region

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