View Clinical Trial (Medical Research Study)

HALO Patient Registry: Ablation of Barrett's Esophagus - NCT00848237-(Clinical Trial 418708)



ClinicalConnection.com has recently undergone an update and this page may no longer be up-to-date. Please Search For Clinical Trials to view the most current clinical trials listings.


Signup
City:  Knoxville and Other Us Cities
State:  
CA
Zip Code:
Conditions: Barrett Esophagus
Purpose: The HALO Patient Registry is a prospective/retrospective, multi-center patient registry. It provides a framework for treatment and follow-up of patients with Barrett's esophagus (non-dysplastic IM, LGD and HGD). The primary objective is to provide a tool for participating physician investigators to collect outcomes data related to the use of the HALO Ablation Systems.
Study summary: Summary The HALO Patient Registry provides a framework for treatment and follow-up of patients with Barrett's esophagus (non-dysplastic IM, LGD and HGD). The primary objective is to provide a tool for participating physician investigators to collect outcomes data related to the use of the HALO Ablation Systems. Protocol Design: This is a prospective, multi-center patient Registry. Sites may choose to also retrospectively enroll previously treated patients (after obtaining informed consent) and enter retrospective data into case report forms on-line. "Retrospective data collection" is defined as any data other than patient history collected prior to signing of the informed consent. A set of case report forms (CRFs) is provided along with this protocol to track outcomes. The CRFs may be completed and retained on site, but the site is recommended to utilize the internet-based data entry system.
Criteria: Inclusion Criteria: - Must be a candidate for ablation of Barrett's esophagus with the HALO Ablation System. - Must agree to the proposed follow-up schedule and provide informed consent for participation. Exclusion Criteria: - Pregnancy - Prior radiation therapy to the esophagus - Esophageal varices at risk for bleeding - Prior Heller Myotomy
Study is available at: Gastrointestinal Associates and sites across the US
Knoxville and Other Us Cities, CA
United States

Primary Contact:
Shirin R Hasan
Email: shasan@barrx.com
Phone: 408-328-7338
If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
Trials Alerts: If you would like to be notified of new clinical trials as they become available please register for a free account.
Data Source: ClinicalTrials.gov
Date Processed: March 23, 2011
Modifications to
this listing:		 Only selected fields are shown, please use the link above to view all information about this clinical trial.