Clinical Trials Logo

Barrett's Esophagus clinical trials

View clinical trials related to Barrett's Esophagus.

Filter by:

NCT ID: NCT02066233 Completed - Barrett's Esophagus Clinical Trials

Prospective Study to Compare the Efficacy of E.G.Scan to Detect Barrett's Esophagus Compared With Standard Endoscopy

Start date: March 2014
Phase: N/A
Study type: Interventional

Will EG Scan (transnasal endoscopy) determine presence of Barrett's Esophagus, esophagitis and hiatal hernia as well as standard sedated endoscopy.

NCT ID: NCT02033070 Not yet recruiting - Barrett's Esophagus Clinical Trials

Patient Registry: Radio Frequency Ablation of Barrett's Esophagus Using HALO System

HALO
Start date: November 2013
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to provide a tool for physicians to compare outcome data related to the use of the HALO Ablation Systems. This study is a single-center patient registry which will contribute to a framework for treatment and follow-up of patients with Barrett's Esophagus.

NCT ID: NCT02018367 Recruiting - Barrett's Esophagus Clinical Trials

Accuracy, Yield and Clinical Impact of a Low-Cost HRME in the Early Diagnosis of Esophageal Adenocarcinoma

Start date: September 2012
Phase: Phase 2
Study type: Interventional

The overall goal of the study is to determine whether imaging with the low-cost High Resolution Microendoscope(HRME) will increase the efficiency and yield of the current standard of endoscopic surveillance of Barrett's esophagus. We believe the HRME will provide an in-vivo "optical biopsy" that will be comparable to gold standard histopathology and allow the endoscopist to make a more informed decision about whether to obtain a biopsy or even perform endoscopic therapy (i.e. endoscopic mucosal resection, EMR).

NCT ID: NCT01976351 Terminated - Barrett's Esophagus Clinical Trials

Imaging Enhanced Endoscopy for the Screening of Barrett's Esophagus

Start date: September 2009
Phase: N/A
Study type: Observational

Imaging enhanced endoscopy can improve the efficacy of screening of Barrett's esophagus and predict its invasiveness. There is potentially molecular change over the Barrett's esophagus in this Chinese population. To evaluate the efficacy of imaging enhanced endoscopy for screening of Barrett's esophagus and evaluation of invasiveness

NCT ID: NCT01961778 Completed - Barrett's Esophagus Clinical Trials

Comparison of Treatments for Barrett's Esophagus With High-Grade Dysplasia/Early Adenocarcinoma

Start date: November 2013
Phase: N/A
Study type: Interventional

Prospective randomized study comparing radiofrequency ablation and cryotherapy for the endoscopic treatment of Barrett's esophagus. The study is powered to assess clinical equivalence (non-inferior) of the treatment regimens.

NCT ID: NCT01913223 Completed - Clinical trials for Colorectal Neoplasms

Endoscopic Sub-mucosal Dissection With the Nestis® Jet Injector System With a Bi-functional Catheter: First Prospective Trial

NESTIS
Start date: June 2012
Phase: N/A
Study type: Interventional

ESD (Endoscopic Sub-mucosal Dissection)is the first-intent method to treat superficial neoplasms of the digestive tract at it allows an en-bloc R0 resection. Following marking of the lesion margins, ESD comprises 3 steps: 1) liquid injection into the sub-mucosal space 2) circumferential (complete or partial) incision and 3) dissection of the submucosa. Several tools are necessary to perform ESD with the standard technique. Development of water jet with bi functional (injection and cutting) catheter allows time and significant reduction of perforation risk (due to multiple changes of instruments). For this purpose, Nestis introduced the Enki 2 pulsed jet technology with high pressure system to inject efficiently and at any time viscous solutions in direct viewing and retroflexion. Preliminary pig studies indicate that injection of glycerol, hyaluronate and hydroxyethlstarch with Enki 2 are possible. In addition, preclinical studies on living pig colon models using saline solutions have demonstrated that perforation rates and operating times are significantly reduced compared to a standard electrosurgical knife. The present clinical study is being performed to confirm this system capability to perform ESD in humans.

NCT ID: NCT01905202 Enrolling by invitation - Barrett's Esophagus Clinical Trials

The Safety and Tolerability of Secretrol in Patients With Barrett's Esophagus

Start date: April 2013
Phase: Phase 1
Study type: Interventional

Secretrol administered over a 6 month period to patients with Barrett's Esophagus will be safe and well tolerated. Further, pH control will be evaluated in the distal esophageal mucosa and just below the squamocolumnar junction.

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: 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: 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.