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Eosinophilic Esophagitis clinical trials

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NCT ID: NCT02202590 Active, not recruiting - Clinical trials for Eosinophilic Esophagitis

Using Spectrally Encoded Confocal Microscopy (SECM) to Image the Esophagus

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

The goal of this study is to test the feasibility and the tolerability of a tethered spectrally encoded confocal microscopy (SECM) capsule and to use it to image the esophagus.

NCT ID: NCT02190513 Completed - Celiac Disease Clinical Trials

Prevalence of Eosinophilic Esophagitis in Children With Celiac Disease

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

Celiac disease (CD) and eosinophilic esophagitis (EE) are distinct diseases of the gastrointestinal tract with specific clinico-pathological characteristics. In recent years, in the literature, several children who underwent upper gastrointestinal endoscopy for suspected CD, which was confirmed histologically, were also found to have coexistent EE. There are reports of coexistent CD and EE. We would like to see the prevalence of EE in children with CD and the prevalence of CD in children with EE in our population, and to do so would like to review medical records. Our objectives are to determine if children with celiac disease have a high prevalence of eosinophilic esophagitis.and to determine if children with eosinophilic esophagitis have increased risk of developing celiac disease.

NCT ID: NCT02125851 Completed - Clinical trials for Eosinophilic Esophagitis

Comparison of Esophageal Clearance Times of Oral Budesonide Preparations

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

The purpose of this study is to determine if a xanthan gum or honey based budesonide slurry exhibit comparable mucosal contact time to a budesonide/sucralose slurry in healthy adult subjects.

NCT ID: NCT02114606 Terminated - Clinical trials for Eosinophilic Esophagitis

Diagnosis and Monitoring of Eosinophilic Esophagitis Using the Cytosponge

Start date: July 2015
Phase: N/A
Study type: Interventional

The current endoscopic methods for diagnosing and monitoring treatment response in Eosinophilic Esophagitis (EoE) are costly, inconvenient, and risky. Novel diagnostic methods are needed, and the minimally-invasive Cytosponge holds great promise. It has been shown to be safe and accurate in Barrett's esophagus, it has the advantage (over the string test) of obtaining a true tissue sample, and our preliminary data supports its further study in EoE. The proposed prospective cohort study, conducted by experts in esophageal diseases and EoE, will assess the accuracy of Cytosponge compared to endoscopy and biopsy in EoE, and determine the safety and acceptability of this technique. Use of the Cytosponge would fundamentally change the paradigm for clinical management of EoE by allowing collection of non-endoscopic esophageal biopsies, thus minimizing the need for invasive testing. It would also facilitate future genetic, mechanistic, and pathogenesis research in EoE.

NCT ID: NCT02113267 Terminated - Clinical trials for Eosinophilic Esophagitis

Mometasone-furoate for Treatment of Eosinophilic Esophagitis - a Randomized Placebo Controlled Study.

Start date: April 2014
Phase: Phase 2
Study type: Interventional

Background: Eosinophilic esophagitis ( EoE ) is a disease entity which has been properly recognized only within the past two decades.(1) A prevalence of nearly 1% means that almost 20,000 people in the Region of Western Sweden may be affected.(2 ) The main symptom is swallowing difficulty and food may be stuck, which typically require acute hospital care with operational action under general anesthesia.( 3,4 ) The standard treatment today is local treatment with steroids by mouth several times a day for a few weeks.( 5 ) In adults and large teenagers, there is only one randomized study which has shown that budesonide has a significant effect exaggerating that of placebo. However, the main end-point in this study was the degree of tissue inflammation.(6) In a separate study using validated questionnaires , we have shown that patients with EoE have distinct organ-specific symptoms and a lowered quality of life . These symptoms nearly disappeared, after treatment with mometasone furoate. However, as that study was not randomized or placebo controlled no causal conclusions could be drawn regarding the treatment effect, but the method of validated questionnaires proved sensitive to changes in symptomatology.(7) Purpose The primary purpose of this study is to evaluate the effect of local steroid treatment with mometasone furoate on swallowing problems in patients with EoE . Secondarily, to evaluate the effect on patient quality of life and the presence of side effects.

NCT ID: NCT02098473 Completed - Clinical trials for Eosinophilic Esophagitis

Dose Ranging Study of RPC4046 in Eosinophilic Esophagitis

Start date: August 31, 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the effective dose(s) of RPC4046 in the treatment of Eosinophilic Esophagitis (EoE). This trial consists of two phases: 16 weeks of double-blind treatment and 52 weeks of open-label extension.

NCT ID: NCT02072590 Completed - Celiac Disease Clinical Trials

Improved Diagnostics of Celiac Disease in Children

Start date: August 2011
Phase:
Study type: Observational

The main purpose of this study is to improve the diagnostics of celiac disease and reduce the need for invasive endoscopic studies in children. Further, the investigators aim to investigate the natural history and risk of complications in children with celiac disease or gluten sensitivity and to create a large scientific database.

NCT ID: NCT02058537 Terminated - Clinical trials for Eosinophilic Esophagitis (EoE)

Bethanechol for Eosinophilic Esophagitis

Start date: February 2014
Phase: Phase 2
Study type: Interventional

The primary goals of this study are to ease the symptoms of patients with Eosinophilic Esophagitis (EoE) and to test the effectiveness of the drug bethanechol in relieving those symptoms.

NCT ID: NCT02038894 Completed - Clinical trials for Eosinophilic Esophagitis

Comparing Anesthetic Techniques in Children Having Esophagogastroduodenoscopies

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

The purpose of this research study is to compare the safety and effectiveness of three commonly used techniques for delivering anesthesia during a procedure known as esophagogastroduodenoscopy.

NCT ID: NCT02019758 Completed - Clinical trials for Eosinophilic Esophagitis

Budesonide Versus Fluticasone for Treatment of Eosinophilic Esophagitis

Start date: January 1, 2015
Phase: Phase 4
Study type: Interventional

Purpose: To determine whether oral viscous budesonide (OVB) or fluticasone metered dose inhaler (MDI) most effectively treats EoE by improving histologic findings and symptoms, which medication provides a more durable treatment response, and whether biomarkers can predict treatment response. Participants: A total of up to 200 16-80 year old patients with a new diagnosis of eosinophilic esophagitis (EoE) who are referred for upper endoscopy will be consented with a target of 122 randomized. Procedures: This will be a prospective, randomized, double-blind, double-dummy, clinical trial comparing OVB to fluticasone MDI for treatment of EoE. This overall study design will generate data for all three Aims