Multi-center Clinical Study to Evaluate the C2 CryoBalloon Focal Ablation System

Exclusion Criteria

• •Non-dysplastic or indefinite for dysplasia BE, confirmed by histopathological analysis
• •Esophageal stenosis/stricture preventing advancement of a therapeutic endoscope (patients may have the stenosis/stricture dilated and then be treated with CryoBalloon ablation under this protocol at a subsequent procedure ≥2 weeks later)
• •Symptomatic untreated strictures
• •Any endoscopically-visualized abnormalities such as ulcers, masses or nodules. Neoplastic nodules must first be treated with EMR ≥6 weeks prior to planned treatment under this protocol.
• •History of esophageal cancer more extensive than T1a or not meeting criteria for low risk of recurrence (confirmed by EMR pathology results negative for positive margin, poorly differentiated carcinoma, and lymphovascular invasion)
• •History of esophageal varices
• •Large (\>4cm) hiatal hernia
• •Prior distal esophagectomy
• •Any clinical or histological suspicion of esophageal adenocarcinoma invading into the submucosa by endoscopic mucosal resection (EMR), or confirmed T1a cancer with positive deep margin by EMR
• •Active esophagitis grade B or higher
• •Severe medical comorbidities precluding endoscopy
• •Uncontrolled coagulopathy
• •Pregnant or planning to become pregnant during period of study participation
• •Patient refuses or is unable to provide written informed consent
• •Life expectancy ≤3 years, as judged by the site investigator
• •General poor health, multiple co-morbidities placing the patient at risk or otherwise unsuitable for trial participation