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Barrett Esophagus clinical trials

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NCT ID: NCT01374074 Completed - Barrett's Esophagus Clinical Trials

Racial Disparity in Barrett's Esophagus

Start date: March 2011
Phase: N/A
Study type: Observational

The goal of the proposed research is to investigate the molecular mechanisms of racial disparity in Barrett's esophagus (BE), the premalignant lesion of esophageal adenocarcinoma. Specifically, the investigators hypothesize that environmental factors, genetic factors, and potentially gene environment interactions play crucial roles in the observed racial disparity in developing Barrett's esophagus. Patients are recruited through UNC hospitals prior to scheduled esophagogastroduodenoscopy (EGD). Participants complete a questionnaire, have body measurements obtained, and have blood, biopsies, and gastric aspirate collected. Participants also complete a 24 hour pH impedance test.

NCT ID: NCT01373125 Completed - Barrett's Esophagus Clinical Trials

Is the Neosquamous Epithelium "Normal" Following Endoscopic Ablation of Dysplastic Barrett's Esophagus?

Start date: June 2011
Phase: N/A
Study type: Observational

The investigators propose a study comparing the morphological and functional aspects of the neosquamous epithelium (NSE) after ablative therapy for dysplastic Barrett's esophagus (BE) to that of native squamous epithelium in normal controls as well as gastroesophageal reflux disease (GERD), non-Barrett's Esophagus (BE) subjects.

NCT ID: NCT01360541 Completed - Low Grade Dysplasia Clinical Trials

Radiofrequency Ablation for Barrett Oesophagus With Low Grade Dysplasia

RF-DBG
Start date: December 22, 2010
Phase: Phase 2
Study type: Interventional

Radiofrequency ablation versus endoscopic surveillance in the management of low grade dysplasia in Barrett oesophagus: a multicentric randomised controlled trial.

NCT ID: NCT01306799 Completed - Barrett's Esophagus Clinical Trials

To Learn How Bone Structure and Bone Mass Change After Long-term PPI Use

BE-CAST
Start date: January 2010
Phase: N/A
Study type: Observational

Patients with severe acid reflux and/or Barrett's esophagus are recommended to take Proton pump inhibitors (PPIs)indefinitely to prevent complications such as strictures or the development of a type of esophageal cancer. Recently, some studies suggested that taking these medications on a long-term basis may affect the bone. Therefore, it is important to learn whether these medications may lead to accelerated bone loss so that effective preventive measures can be developed for patients who require these medications for acid-related conditions. Several studies reported that patients receiving PPIs for many years may have increased risk of hip fractures. However, it is unclear whether this is because the PPIs cause reduced bone density or whether the increased risk of fractures has nothing to do with PPIs and is because patients who require PPIs have other illnesses that cause the increased fractures. The purpose of the study is to learn how bone structure and bone mass change after long-term PPI use.

NCT ID: NCT01298999 Completed - Barrett's Esophagus Clinical Trials

Trial of a Gastrin Receptor Antagonist in Barrett's Esophagus

Start date: June 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether treatment with an experimental drug called YF476 in patients with Barrett's esophagus reduces the expression of tissue markers that are associated with an increased risk of developing esophageal cancer.

NCT ID: NCT01293448 Completed - Esophageal Cancer Clinical Trials

Evaluation of Balloon-based Cryoablation of Human Esophageal Epithelium

Start date: December 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate a cryoablation technique used to ablate human esophageal mucosa.

NCT ID: NCT01288612 Completed - Barrett's Esophagus Clinical Trials

Comparative Effectiveness of Endoscopic Assessment of Gastroesophageal Reflux and Barretts Esophagus

challenge
Start date: February 2011
Phase: N/A
Study type: Interventional

The hypothesis of this study was that the comparative effectiveness of unsedated transnasal endoscopy (uTNE) will be greater than sedated endoscopy (sEGD) in population screening for BE.

NCT ID: NCT01286155 Completed - Barrett's Esophagus Clinical Trials

Epidemiology of Barrett's Esophagus: A Population Based Study

Start date: January 2010
Phase: N/A
Study type: Observational

To assess attitudes toward screening for esophageal adenocarcinoma (EAC) and Barrett's esophagus (BE) in the community. To develop a population based clinical risk factor prediction model for the diagnosis of BE and identify novel risk factors for BE which would make population based screening more efficient. This will be an important first step in identifying the target population for BE screening, another crucial component of making screening feasible and efficient

NCT ID: NCT01281618 Completed - Barrett's Esophagus Clinical Trials

Influence of Acid Reflux on Stromal Epithelial Interaction in Barrett's Esophagus

CR20
Start date: October 2008
Phase: N/A
Study type: Observational

The purpose of this study is to determine the association between acid reflux and cell changes in Barrett's esophagus. Specific aim 1: To test the hypothesis that controlled acid reflux is associated with lesser degree of stromal activation. Specific aim 2: To test the hypothesis that stromal fibroblast derived growth factors drive BE epithelial proliferation.

NCT ID: NCT01238042 Completed - Barrett's Esophagus Clinical Trials

Study To Determine The Maximum Range of Light Doses At Two HPPH Doses With Acceptable Normal Tissue Toxicity For PDT Treatment Of High Grade Dysplasia,CIS or Early Adenocarcinoma In Barrett's Esophagus

Start date: March 2003
Phase: Phase 1
Study type: Interventional

Patient's with High Grade Dysplasia, Carcinoma in situ or Early Adenocarcinoma in Barrett's Esophagus are injected with HPPH and one day later are endoscopically treated with light from a laser.