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临床试验/NCT05751824
NCT05751824尚未招募不适用

Evaluating the Effect of the Automatic Surveillance System on Surveillance Rate of Colorectal Postpolypectomy Patients: A Prospective, Multicenter Study

Renmin Hospital of Wuhan University2 个研究点 分布在 1 个国家目标入组 867 人开始时间: 2023年2月26日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
867
试验地点
2
主要终点
surveillance rate

研究概览

简要总结

In this study, we proposed a prospective study about the effect of the automatic surveillance system on surveillance rate of colorectal postpolypectomy patients. The enrolled patients were divided into group A with intelligent surveillance system, group B with manual reminder, and group C with natural state. The surveillance among the three groups were compared.

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
Double (Participant, Care Provider)

入排标准

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

入选标准

  • Male or female aged 18 years or older who undergo colonoscopy.

排除标准

  • No pathological result.
  • No or invalid contact information.
  • The surveillance interval cannot be determined according to the surveillance guidelines, including poor bowel preparation, colorectal cancer or suspicious malignance, surgery or colorectal ESD history, those who fail to complete colonoscopy due to unbearable, pathological indications of not polyps, hamartoma or lymphoma polyps, history of ulcerative colitis, and so on.
  • Has participated in other clinical trials, signed the informed consent form and is in the surveillance period of other clinical trials.
  • Have drug or alcohol abuse or psychological disorder in the past five years.
  • 6)Pregnancy.
  • 7)Not suitable for recruitment after investigator evaluation because of other high-risk conditions.

结局指标

主要结局

surveillance rate

时间窗: From enrollment to study completion, assessed up to 3 years.

The numerator is the number of patients with surveillance, and the denominator is the number of all colorectal postpolypectomy patients requiring surveillance.

次要结局

  • lesion regression rate(From enrollment to study completion, assessed up to 3 years.)
  • The accuracy of identifing post-polypectomy patients(At the time of enrollment.)
  • The incidence rate of colorectal cancer(From enrollment to study completion, assessed up to 3 years.)
  • Advance Surveillance Rate(From enrollment to study completion, assessed up to 3 years.)
  • On-time Surveillance Rate(From enrollment to study completion, assessed up to 3 years.)
  • The accuracy of classifying risk levels(At the time of enrollment.)
  • The accuracy of assigning surveillance intervals(At the time of enrollment.)
  • lesion progression rate(From enrollment to study completion, assessed up to 3 years.)
  • Delayed Surveillance Rate(From enrollment to study completion, assessed up to 3 years.)
  • lesion persistence rate(From enrollment to study completion, assessed up to 3 years.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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