跳至主要内容
临床试验/NCT06030180
NCT06030180已完成不适用

CLUE: CLinical Utility Study of EsoGuard on Samples Collected Using EsoCheck as a Triage Test for Endoscopy to Identify Barrett's Esophagus (BE)

Lucid Diagnostics, Inc.16 个研究点 分布在 1 个国家目标入组 566 人开始时间: 2023年2月23日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
566
试验地点
16
主要终点
Clinical Utility

研究概览

简要总结

Utilize real-world data from the commercial use of EsoGuard testing on samples collected with EsoCheck (EC/EG) to evaluate the impact of EsoGuard results on health care provider's decision for endoscopy referral. Assess patient compliance with recommendations for upper endoscopy, and relationship of compliance to positive EsoGuard results.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
12 Years 至 99 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Individuals in whom the clinical decision has been made to screen for BE using EC/EG
  • Individuals who meet criteria for BE screening in accordance with either the 2022 ACG guidelines, or the AGA best practice advice from their 2022 clinical practice update.

排除标准

  • Individuals who fall outside the eligible population defined by the EsoCheck device Instructions For Use (IFU)
  • Individuals who do not meet either the ACG or AGA guidelines/practice advice for BE screening
  • Inability to provide written informed consent or participate in the required follow up

结局指标

主要结局

Clinical Utility

时间窗: Through study completion, an average of 1 year

Utilize real-world data from the commercial use of EsoGuard testing on samples collected with EsoCheck (EC/EG) to evaluate the impact of EsoGuard results on health care provider's decision for endoscopy referral. This will be measured by asking physicians how the EsoGuard result impacted their referral decision.

次要结局

  • Patient Compliance(Through study completion, an average of 1 year)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (16)

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