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临床试验/NCT02729753
NCT02729753已完成不适用

Clinical Study to Evaluate the CryoBalloon™ Full and Swipe Ablation Systems for Ablation of Human Esophageal Epithelium

Pentax Medical4 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2016年4月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
4
主要终点
Safety of the CryoBalloon™ Full and Swipe Ablation System

研究概览

简要总结

This study will evaluate the C2 CryoBalloon™ Full and Swipe Ablation Systems for the ablation of human esophageal epithelium in patients scheduled to undergo esophagectomy for reasons unrelated to the objective of the study

详细描述

The primary outcomes for the study are the safety and treatment effect of the C2 CryoBalloon™ Ablation System. An esophagectomy will be performed as scheduled following the ablation procedure; histopathological analysis of surgically-resected specimens will be performed.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Basic Science
盲法
None

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

  • Minimum of one 3cm area of non-ulcerated columnar-lined esophagus or squamous-lined tissue suitable for ablation
  • Older than 18 years of age
  • Requires a clinically necessary esophagectomy for esophageal cancer or other indications.

排除标准

  • Patient has esophageal narrowing limiting access to the intended sites of ablation

结局指标

主要结局

Safety of the CryoBalloon™ Full and Swipe Ablation System

时间窗: 2 weeks

Number of participants with serious, device-related adverse events after treatment with the CryoBalloon™ Swipe Ablation System

Effect of Ablation to Submucosa at Different Depth of Tissue Ablation Using the CryoBalloon™ Full and Swipe Ablation Systems

时间窗: 2 weeks

Evaluated by depth and uniformity of ablation effect in the esophagus based on histopathologic assessment. Dose response by effect of ablation to submucosa: 0: Normal 1. Inflammatory cell infiltration 2. Separation with inflammation 3. Edema and Necrosis

次要结局

  • Device Performance: Average Procedure Time(Minutes from start to end of procedure)
  • Device Performance: Ease of Deployment of Device(Minutes, from start to end of procedure)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (4)

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