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Cryotherapy Ablation of Barrett's Esophagus and Early Esophageal Cancer
The purpose of this study is to confirm the effectiveness and safety of a new medical device which sprays liquid nitrogen through an upper endoscope (cryotherapy) to treat Barrett's esophagus with high-grade dysplasia and early esophageal cancer. It is hypothesized that this treatment will remove the abnormal lining of the esophagus and allow the normal esophageal lining to return.
Barrett's esophagus (BE) with high grade dysplasia (HGD) is a precursor of esophageal adenocarcinoma. Eliminating this condition may control the current rapid rise of adenocarcinoma. Ablative techniques are attempted to avoid the high morbidity and mortality of esophagectomy or for use in patients who cannot undergo surgery. Current ablative techniques have achieved mucosal ablation with variable success but are associated with high cost, patient discomfort and/or significant complications. A novel device which sprays liquid nitrogen through an upper endoscope (cryotherapy) has been shown to be a safe and effective procedure to ablate the esophageal mucosa in swine and dog models and in pilot studies in humans. Successful reversal of BE, LGD, HGD and superficial adenocarcinoma and squamous cell carcinoma have been demonstrated when cryotherapy with this device is followed by healing of the esophageal lining in a low acid environment. This study is undertaken to demonstrate the efficacy and safety in the ablation of Barrett's esophagus with high-grade, neoplasia, and severe esophageal squamous dysplasia and to confirm preliminary results in humans.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
University of Maryland School of Medicine and Greenebaum Cancer Center
Baltimore, Maryland, United States
Start Date
April 1, 2006
Primary Completion Date
May 1, 2007
Completion Date
May 1, 2007
Last Updated
February 8, 2022
23
ACTUAL participants
CSA System (CryoSpray AblationTM System)
DEVICE
CryoSpray Ablation
DEVICE
Lead Sponsor
University of Maryland, Baltimore
Collaborators
NCT07267468
NCT05753748
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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