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Barrett Esophagus clinical trials

View clinical trials related to Barrett Esophagus.

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NCT ID: NCT01882478 Completed - Clinical trials for Early Esophageal Adenocarcinoma Post Radio Frequency Ablation

Cryotherapy -BEATS-RF Ablation Trial

Start date: June 2013
Phase:
Study type: Observational

The purpose of this study is to determine whether cryotherapy is effective in the treatment of persistent high grade dysplasia (HGD) or early esophageal adenocarcinoma (IMCA) in patients who have not responded to radiofrequency ablation (RFA).

NCT ID: NCT01845454 Terminated - Barrett's Esophagus Clinical Trials

A Dose-Optimization Study for the Initial Treatment of Dysplastic Barrett's Esophagus With trūFreeze™ Spray Cryotherapy

DOSE
Start date: April 2013
Phase: N/A
Study type: Interventional

The primary objective of this study is to determine the percentage segment regression after spray cryotherapy in a dose-escalation study performed in patients with dysplastic Barrett's Esophagus (BE) using trūFreeze™ spray cryotherapy within the currently recommended therapeutic range. Secondary objectives are the determination of safety related outcomes such as esophageal stricture.

NCT ID: NCT01802203 Completed - Barrett Esophagus Clinical Trials

trūFreeze® Spray Cryotherapy Patient Registry

Start date: April 2013
Phase:
Study type: Observational [Patient Registry]

To collect efficacy and outcomes data related to the use of trūFreeze® spray cryotherapy for the treatment of unwanted tissue in the pulmonary and gastrointestinal settings.

NCT ID: NCT01787864 Completed - Barrett's Esophagus Clinical Trials

Prevalence of Dysplasia of the Gastric Cardia

Start date: February 2013
Phase: N/A
Study type: Observational

We propose a tissue sample collection study for patients at UNC who have undergone or will undergo radiofrequency ablation therapy for Barrett's Esophagus (BE) or intramucosal adenocarcinoma as part of routine medical care. Purpose: To determine the prevalence of metaplasia and dysplasia in the gastric cardia before and after ablative therapy. To determine the incidence of cardiac metaplasia and dysplasia as a function of ablative therapy. To determine the correlation between dysplasia in the tubular esophagus, and dysplasia in the cardia. To assess the ability of immunohistochemical (IHC) staining of cardia tissues to predict incident dysplasia in the cardia. Several well-characterized biomarkers, including p16, p53, Ki67, cyclin D1, and cyclin A, will be assessed.

NCT ID: NCT01776346 Recruiting - Clinical trials for Gastroesophageal Reflux

Barrett's Esophagus Patient Registry

BPR
Start date: January 2011
Phase: N/A
Study type: Observational [Patient Registry]

The ultimate goal of the Barrett's Esophagus Patient Registry is to help develop more effective targeted screening strategies and treatment options for Barrett's esophagus and esophageal adenocarcinoma (EAC). We plan to do by developing a registry that will serve as a platform. Examples of analyses could include identifying genetic determinants and biomarkers that predict BE, progression of BE to EAC, as well as the response to therapies.

NCT ID: NCT01733719 Completed - Barretts Esophagus Clinical Trials

Barrett&Apos;s Intervention for Dysplasia by Endoscopy

BRIDE
Start date: February 2013
Phase: N/A
Study type: Interventional

LAY SUMMARY A type of gullet cancer (oesophageal adenocarcinoma) has become the 5th commonest UK cause of cancer death. Unfortunately, by the time patients have symptoms, the cancer is often incurable. People with Barrett's oesophagus (change of gullet lining occurring in some with acid reflux) at risk of this cancer can have regular check-ups, involving examination through an endoscope (an instrument inserted by mouth, under mild sedation if required). A small proportion of people with Barrett's develop further changes (which might become cancer) in the gullet lining; if they do, it is important to remove the affected tissue before cancer develops, or when it is at an early stage. There are several ways of removing this tissue but the investigators do not know which is best. The standard treatment is surgery, but there is a small risk of dying from the operation, and patients often suffer complications affecting them for a year or more afterwards. Two endoscopic treatments do not involve surgery. Both involve removing visible abnormalities by a technique called endoscopic resection, followed by cauterising the remaining Barrett's gullet lining by 1 of 2 techniques. One is recommended by the National Institute for Health and Clinical Excellence, but it is expensive and less widely available than the second. No-one has compared these treatments with each other, nor with surgery, in randomised trials (the most reliable way of deciding which is best). Patient groups say they would prefer to avoid surgery if the alternative works, and have encouraged us to do trials. This feasibility study is a vital step towards two trials: (a) a trial to compare the two non-surgical techniques and (b) a trial comparing surgery with endoscopic treatment. It will help us find out whether it will be possible to enroll and retain enough patients by using several centres, and to identify/resolve any other potential barriers to recruitment and retention, including exploring viewpoints of patients and surgeons.

NCT ID: NCT01733147 Completed - Obesity Clinical Trials

Modulation of Esophageal Inflammation in Barrett's Esophagus by Omega-3 Fatty Acids

Start date: November 2012
Phase: Phase 4
Study type: Interventional

This study is being done to understand the effect of dietary omega-3 fats in decreasing tissue inflammation in Barrett's esophagus.

NCT ID: NCT01694511 Completed - Barrett's Esophagus Clinical Trials

Endoscopic Detection of Dysplasia in Barrett's Esophagus

Start date: November 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether High Resolution Magnification Endoscopy (HRME) and Computed Virtual Chromoendoscopy (CVC) with targeted biopsies is superior to conventional white light endoscopy (WLE) with 4 quadrant biopsies of the metaplastic epithelium every 1-2 cm (Seattle Protocol) for detection of pre-malignant lesions in patients with Barrett's Esophagus (BE).

NCT ID: NCT01641887 Not yet recruiting - Esophageal Cancer Clinical Trials

Decision Aid for Gastroesophageal Reflux Disease Management

Start date: January 2014
Phase: N/A
Study type: Observational

The study is to test a decision aid that is designed to help patients make decision regarding management of their gastroesophageal reflux disease (GERD). Once the decision aid is constructed we will test and assess the aid on ~100 patients who have GERD to assess effectiveness.

NCT ID: NCT01633411 Completed - Barrett's Esophagus Clinical Trials

Evaluation of Effect of CryoBalloon Focal Ablation System on Human Esophageal Barrett's Epithelium

Start date: December 2011
Phase:
Study type: Observational

This is a feasibility study without a primary study hypothesis or statistical comparison.