CryoSpray Ablation (TM) GI Patient Registry

NCT00747448 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 199

Last updated 2016-02-02

No results posted yet for this study

Summary

The purpose of this study is to create a patient registry to collect and analyze post-510K approval information on subjects treated endoscopically with the CryoSpray Ablation™ System.

Conditions

  • Barrett's Esophagus
  • Esophageal Cancer

Sponsors & Collaborators

  • CSA Medical, Inc.

    lead INDUSTRY

Principal Investigators

  • Ann Murphy Legg, RN · CSA Medical, Inc.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-05-31
Primary Completion
2013-06-30
Completion
2013-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00747448 on ClinicalTrials.gov