Esophageal Cancer Clinical Trial

Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium

Summary

The purpose of this study is to evaluate a cryoablation technique used to ablate human esophageal mucosa.

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Full Description

The purpose of this study is to evaluate the histological results of a cryoablation technique used to ablate human esophageal mucosa. The performance and safety of the cryoablation technique will also be evaluated.

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Eligibility Criteria

Inclusion Criteria:

Patient must have a minimum of 2.0 cm of non-ulcerated, non-inflammatory columnar-lined esophagus or squamous esophageal lined tissue suitable for ablation. A patient may be treated with up to 2 zones of ablation.
Patient is 18 to 80 years of age at the time of consent (inclusive).
Patient has provided written Informed Consent Form (IFC) using a form that has been approved by the Institution's reviewing IRB/EC.
Patient is willing and able to comply with all Clinical Investigation Plan (CIP) requirements.
Patient's esophagectomy is clinically necessary due to reasons unrelated to this study.
Patient is deemed operable per standard institutional criteria.

Exclusion Criteria:

Patient has a known history of unresolved drug or alcohol dependency that would limit ability to comprehend or follow instructions related to IFC, post treatment instructions or follow-up guidelines.
Patient refuses or is unable to provide written informed consent. - -
Patient has or is currently undergoing endoscopic ablation therapy within 4 cm from the proposed treatment area including, but not limited to cryospray therapy, laser treatment, photodynamic therapy, multi-polar electro coagulation, endoscopic mucosal resection, radiofrequency ablation or argon plasma coagulation.
Patient has esophageal narrowing limiting access to the intended site of ablation.
Patient is undergoing or has recently undergone chemotherapy (within 15 days or WBC below normal by institutional criteria or standards).
Patient is undergoing or has recently undergone radiation therapy which involved the esophagus (within 15 days or WBC below normal by institutional criteria or standards).

Study is for people with:

Esophageal Cancer

Estimated Enrollment:

21

Study ID:

NCT01293448

Recruitment Status:

Completed

Sponsor:

Pentax Medical

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There are 4 Locations for this study

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University of Southern California
Los Angeles California, 90033, United States
University of Rochester
Rochester New York, 14642, United States
University of Pittsburgh
Pittsburgh Pennsylvania, 15232, United States
AMC
Amsterdam AZ, 1105, Netherlands

How clear is this clinincal trial information?

Study is for people with:

Esophageal Cancer

Estimated Enrollment:

21

Study ID:

NCT01293448

Recruitment Status:

Completed

Sponsor:


Pentax Medical

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