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Barrett Esophagus clinical trials

View clinical trials related to Barrett Esophagus.

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NCT ID: NCT05216133 Enrolling by invitation - Clinical trials for Gastroesophageal Reflux Disease

Biomarkers of Airway Disease, Barrett's and Underdiagnosed Reflux Noninvasively (BADBURN)

Start date: March 22, 2023
Phase:
Study type: Observational

A majority of Fire Department of New York (FDNY) World Trade Center (WTC) exposed rescue and recovery workers developed gastroesophageal reflux disease (GERD), a risk factor for Barrett's Esophagus (BE) and subsequent esophageal cancer. There is diminished health-related quality of life and productivity associated with aerodigestive diseases such as GERD and BE. This proposal will leverage the longitudinally phenotyped WTC exposed cohort, validate biomarkers of WTC-aerodigestive disease, and develop novel, noninvasive disease phenotyping of premalignant diseases such as BE, and identify potential targeted therapeutics to improve care.

NCT ID: NCT04561791 Enrolling by invitation - Barrett Esophagus Clinical Trials

Evaluation of Tethered Capsule Endomicroscopy as a Screening Tool for Barrett's Esophagus in the Primary Care Setting

Start date: January 2, 2019
Phase: N/A
Study type: Interventional

The investigators will conduct a large study in the primary care clinic to determine the feasibility of using tethered capsule endomicroscopy as a screening method for Barrett's esophagus (BE) in the primary care practice environment. The investigators are also determining the prevalence of Barrett's esophagus in a primary care practice cohort at MGH.

NCT ID: NCT04457193 Enrolling by invitation - Barrett Esophagus Clinical Trials

Outcomes After Transoral Incisionless Fundoplication (TIF) Following Successful Endoscopic Ablation for Barrett's Esophagus

Start date: June 7, 2018
Phase:
Study type: Observational

Barrett's esophagus (BE) is a precancerous lesion characterized by the replacement of the normal stratified squamous epithelium of the distal esophagus by intestinal metaplasia (IM). Non-dysplastic BE may progress to low-grade dysplasia (LGD), to high-grade dysplasia (HGD) and esophageal adenocarcinoma (EAC). Endoscopic ablation is safe and effective for complete eradication of BE. However, recurrence is common. Cumulative incidence rate of BE recurrence is up to 30% in the third year. Thus, achieving complete eradication of IM, patients should undergo surveillance indefinitely with serial endoscopy to assess for recurrence of BE. In addition, BE patients have been committed to life-long proton pump inhibitor (PPI) therapy, but increasing concerns about adverse effects has led to alternative therapies. Studies have showed that laparoscopic Nissen fundoplication may decrease recurrence of BE after endoscopic ablation. Transoral Incisionless Fundoplication (TIF) is an endoscopic procedure that mechanically creates fundoplication similar to traditional operative Nissen fundoplication. The role of TIF in patients with BE whom underwent successful endoscopic ablation has not been fully investigated.

NCT ID: NCT03853772 Enrolling by invitation - Clinical trials for Gastroesophageal Reflux Disease

The Johns Hopkins Heartburn Center Registry

Start date: April 27, 2019
Phase:
Study type: Observational [Patient Registry]

A multi-center, multi-year registry of patients with gastroesophageal reflux disease (GERD) undergoing diagnostic evaluation and/or treatment of GERD and associated diseases and complications.

NCT ID: NCT03311451 Enrolling by invitation - Barrett Esophagus Clinical Trials

C2 CryoBalloon™ 180 Ablation System Dose De-escalation Study.

Start date: January 16, 2023
Phase: N/A
Study type: Interventional

The primary objective is to determine the safety, performance and efficacy of the C2 CryoBalloon 180 Ablation System ("CryoBalloon 180") used at decreasing doses in treatment naïve patients with low- or high-grade dysplastic Barrett's Esophagus (BE) or with residual BE after resection of dysplasia or early adenocarcinoma.

NCT ID: NCT02427269 Enrolling by invitation - Esophageal Cancer Clinical Trials

University of North Carolina (UNC) Barrett's Esophagus and Esophageal Cancer Biorepository

BEECAB
Start date: April 28, 2015
Phase:
Study type: Observational

Aim 1: To develop a prospective tissue and blood biorepository from patients with a history of Barrett's Esophagus (BE) or esophageal cancer (ECA) presenting to UNC hospitals for routine care upper endoscopy for their condition. Aim 2: To collect clinical data from patients with a history of Barrett's Esophagus (BE) or esophageal cancer (ECA) that includes demographic data, endoscopic procedure data, and pathology data. Aim 3: To integrate Aim 1 and 2 in a manner that will provide an efficient bi-directional flow of clinical information and specimens between laboratory and clinical scientists in order to foster innovative translational research. Aim 4: To create a biorepository for future Institutional Review Board (IRB) approved studies that have tissue and/or blood specimen component.

NCT ID: NCT02149914 Enrolling by invitation - Barrett's Esophagus Clinical Trials

The Changes of Ryodoraku and HRV After PPI Treatment in GERD Patients

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

Gastroesophageal reflux disease(GERD) mainly related to the reflux of stomach content induced by the dysfunction of lower esophageal sphincter. Proton pump inhibitors (PPI) can effectively block gastric acid secretion but the drug reactions and the degree of improvement in symptoms are sometimes unpredictable. The aim of this study is to investigate the association between the clinical efficacy of PPI in patients with GERD and the personal physical status by Ryodoraku and ANSWatch.

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: NCT00587314 Enrolling by invitation - Barrett's Esophagus Clinical Trials

The Effect of Ablation Therapy on Barrett's Esophagus

ablation IN BE
Start date: January 2004
Phase:
Study type: Observational

To assess the effect of ablative therapy (Photodynamic Therapy or Radiofrequency ablation ) on Barrett's Esophagus