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Clinical Trials/NCT02729753
NCT02729753
Completed
Not Applicable

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

Pentax Medical2 sites in 1 country10 target enrollmentApril 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Esophageal Cancer
Sponsor
Pentax Medical
Enrollment
10
Locations
2
Primary Endpoint
Safety of the CryoBalloon™ Full and Swipe Ablation System
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

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

Detailed Description

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.

Registry
clinicaltrials.gov
Start Date
April 2016
End Date
October 30, 2016
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 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.

Exclusion Criteria

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

Outcomes

Primary Outcomes

Safety of the CryoBalloon™ Full and Swipe Ablation System

Time Frame: 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

Time Frame: 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

Secondary Outcomes

  • 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)

Study Sites (2)

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