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Clinical Trial Summary

The purpose of this study is to evaluate the safety and effectiveness of the CryoSpray Ablation System to treat esophageal low grade dysplasia (LGD) or high grade dysplasia (HGD) within Barrett's Esophagus (BE).


Clinical Trial Description

The study will consist of an estimated 200 subjects with HGD or LGD within BE who are deemed inoperable or refuse standard surgical treatment. A maximum of 20 investigational sites will participate with a maximum of ten subjects per site. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00526786
Study type Interventional
Source CSA Medical, Inc.
Contact
Status Terminated
Phase Phase 4
Start date September 2007
Completion date September 2009

See also
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