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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00939263
Other study ID # 231/08
Secondary ID 0901
Status Recruiting
Phase N/A
First received July 13, 2009
Last updated September 15, 2015
Start date January 2011
Est. completion date December 2016

Study information

Verified date September 2015
Source University Hospital Inselspital, Berne
Contact Ekaterina Safroneeva, PhD
Phone +41 31 631 59 71
Email esafroneeva@ispm.unibe.ch
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial Summary

Eosinophilic Esophagitis (EoE) is a chronic inflammatory disease of the esophagus affecting children and adults. The most frequent symptoms are swallowing difficulties and thoracic pain. The disease has first been described in the 1980s and is found with rapidly increasing frequency mainly in industrialized countries. The factors that lead to EoE are until now incompletely understood, of importance, the disease is found more frequently in men and patients suffering from allergic diseases (e.g., Asthma). So far there exists no activity index to define the severity of EoE; such an index is urgently needed for future clinical trials to determine the efficacy of current and future therapies. The investigators' 3-year project, carried out in cooperation with international EoE experts, aims at the development of an activity index for adult and pediatric EoE patients that will be used in future clinical trials as well as observational studies.


Description:

Background:

1. Introduction Coordinated by the Swiss Eosinophilic Esophagitis Research Group and in close collaboration with The International Gastrointestinal Eosinophil Researchers (TIGERS), we plan to conduct a series of related studies in order to develop an Activity Index (AI) for adult and pediatric patients with Eosinophilic Esophagitis (EoE).

EoE is an emerging disease, with rapidly growing clinical relevance and research activities. A validated assessment instrument is therefore urgently needed.

The purpose of this project is to develop within a representative group of pediatric and adult EoE-experienced gastroenterologists and EoE-experienced pathologists an AI for this chronic inflammatory esophageal disease. The project is investigator initiated, but funding from different sources will be necessary. The project will be conducted in compliance with this protocol, with the ICH guideline E6 on Good Clinical Practice, the FDA perspectives on patient-reported outcomes to support medical product labeling claims (1,2), and the applicable regulatory requirements.

As EoE is a new disorder we include below a comprehensive description of the disease.

1.1. Characterization of Eosinophilic Esophagitis Definition: EoE is rapidly emerging as a distinctive disorder in pediatric and adult gastroenterology. EoE is a chronic-inflammatory esophageal disease, characterized clinicopathologically by the presence of esophagus-related symptoms and by a dense esophageal eosinophilia, both of which persist despite prolonged treatment with proton pump inhibitors (3). Epidemiology: EoE is diagnosed 2-3 times more frequently in males than in females.

The disease is found mainly in industrialized countries such as the United States, Canada, Europe and Australia. EoE is likely to be a 'young' disease: it had not been seen prior to the early 1980, and there is strong evidence to suggest that its prevalence is increasing (4)(5). A population-based study performed in Switzerland suggested an increase in prevalence from 2 per 100000 to 40 per 100000 inhabitants over a 19-year period (6). Clinical Symptoms: As in many other diseases, symptom presentation differs significantly between children and adults. In infants and toddlers, food refusal is a common symptom of EoE. Children often suffer from GERD-like symptoms, vomiting and abdominal pain. Dysphagia and food impaction are reported increasingly with proceeding age. Adolescents and adults present mostly with dysphagia for solids and food impaction (5-7). Endoscopy/Histology: Esophago-gastro-duodenoscopy (EGD) is the first diagnostic step in the evaluation of an individual with suspected EoE. A broad spectrum of endoscopic features associated with EoE have been described, but the endoscopic suspicion needs confirmation by histology. The key diagnostic criterion for diagnosing EoE is an increased number of intraepithelial eosinophils in patients with lack of responsiveness to high-dose proton pump inhibition or normal pH-monitoring of the distal esophagus. In a consensus conference a cut-off value of =15 Eos/HPF (peak eosinophilic count in 400 fold magnification) in any biopsy was recommended as diagnostic criterion (3). Treatment: The optimal treatment for EoE is not yet clear, as experience has been limited largely to case series and small controlled trials. So far topically and systemically administered corticosteroids, several types of allergen-reduced diets, immunosuppressants and IL-5 blocking agents have been shown to be efficacious (8-11).

1.2. Rationale for the planned Studies In the clinical setting the current status of a given disease is often reported as "mild", "moderate" and "severe", and the course of the disease over time is described with terms such as "stable", "progressive", "in remission" or "flare-up". None of these terms has so far been clearly defined for EoE. However, an increasing number of phase 3 therapeutic multi-center trials and natural history studies in patients with EoE will be performed in the near future. In order to set up standardized study protocols and to compare results between different studies a standardized definition of disease activity is a necessity. Taken together, for clinical and for research purposes it is indispensable to define the terms mentioned above by a suitable, reproducible and validated score, which reflects the disease activity as precisely as possible. The necessity for such a score has repeatedly been discussed by the TIGERS and has been underscored by several publications (12).

Objective

The planned research program has the aim to develop and validate an AI for EoE (EEsAI) for adult (adEEsAI) and pediatric (pedEEsAI) patients, which can be used in future clinical trials and observational studies. According to the characterization of EoE, the AI will likely contain clinical and histopathological items. Laboratory and endoscopical parameters may be part of the score, but in a subsidiary role.

Methods:

The development and validation of a disease activity index is a research program involving several related studies. Broadly speaking, it involves 3 main steps: Step I Item Generation and Reduction through a Delphi process with an international expert group (Development phase A). Step II Item Weighting and Activity Index Derivation, using data from a first cohort of adult and a first cohort of pediatric patients (Development phase B).

Step III Evaluation of the Activity Index using data from a second independent cohort of adult and pediatric patients respectively. This involves also assessment of test-retest reliability and responsiveness of the score, using longitudinal data from the same patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 650
Est. completion date December 2016
Est. primary completion date July 2016
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- every patient with the diagnosis Eosinophilic Esophagitis

- pediatric and adult EoE patients

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Intervention

Other:
assessment of disease activity using the EEsAI
disease activity index

Locations

Country Name City State
Canada Clinical Epidemiology & Biostatistics : Mc Master University Hamilton Ontario
Canada Ste-Justine Hospital : University of Montreal Montréal Quebec
Switzerland Department of Gastroenterology, Inselspital/Bern University Hospital Bern
Switzerland Institute for Social and Preventive Medicine, University of Bern Bern
Switzerland Pädiatrische Gastroenterologie Medizinische Universitäts-Kinderklinik Bern Bern
Switzerland University Hospital Lausanne (CHUV) Lausanne
Switzerland Department of Gastroenterology and Hepatology, Kantonsspital Lucerne Lucerne
Switzerland Institute for Pathology, Kantonsspital Lucerne Lucerne
Switzerland Praxis Römerhof, Römerstr. 7, Olten Olten
Switzerland Ostschweizer Kinderspital St. Gallen
United Kingdom Northumbria Healthcare Foundation Trust North Tyneside Hospital North Shields
United States The Children`s Hospital : University of Colorado Denver Aurora Colorado
United States Institute for Clinical Research and Health Policy Studies: Tufts Medical Center Boston Massachusetts
United States Division of Allergy and Inflammation : Harvard Medical School Boston Brookline Massachusetts
United States Division of Gastroenterology : Northwestern University Chicago Chicago Illinois
United States Gastroenterology, hepatology and nutrition : Ann & Robert H. Lurie Children's Hospital of Chicago Chicago Illinois
United States Gastroenterology, Hepatology and Nutrition : University of Cincinnati Cincinnati Ohio
United States Inova Fairfax Hospital for Children Fairfax Virginia
United States Riley Hospital for Children : Indiana University School of Medicine Indianapolis Indiana
United States Gastroenterology and Hepatology : Mayo Clinic, Jacksonville Jacksonville Florida
United States Pediatrics : Mount Sinai School of Medicine New York New York
United States Children`s Hospital of Philadelphia : University of Philadelphia Philadelphia Pennsylvania
United States Mayo Clinic Rochester Rochester Minnesota
United States Department of Pediatrics : University of California San Diego California
United States Gastroenterology and Hepatology : Mayo Clinic, Scottsdale Scottsdale Arizona

Sponsors (10)

Lead Sponsor Collaborator
University Hospital Inselspital, Berne Indiana University School of Medicine, Kantonsspital Olten, Luzerner Kantonsspital, Mayo Clinic Rochester, Minnesota, USA, Northwestern University, Philadelphia University, University of Bern, University of Cincinnati, University of Colorado, Denver

Countries where clinical trial is conducted

United States,  Canada,  Switzerland,  United Kingdom, 

References & Publications (8)

Furuta GT, Liacouras CA, Collins MH, Gupta SK, Justinich C, Putnam PE, Bonis P, Hassall E, Straumann A, Rothenberg ME; First International Gastrointestinal Eosinophil Research Symposium (FIGERS) Subcommittees. Eosinophilic esophagitis in children and adults: a systematic review and consensus recommendations for diagnosis and treatment. Gastroenterology. 2007 Oct;133(4):1342-63. Epub 2007 Aug 8. Review. — View Citation

Guyatt GH, Deyo RA, Charlson M, Levine MN, Mitchell A. Responsiveness and validity in health status measurement: a clarification. J Clin Epidemiol. 1989;42(5):403-8. — View Citation

Liacouras CA, Spergel JM, Ruchelli E, Verma R, Mascarenhas M, Semeao E, Flick J, Kelly J, Brown-Whitehorn T, Mamula P, Markowitz JE. Eosinophilic esophagitis: a 10-year experience in 381 children. Clin Gastroenterol Hepatol. 2005 Dec;3(12):1198-206. — View Citation

Noel RJ, Putnam PE, Rothenberg ME. Eosinophilic esophagitis. N Engl J Med. 2004 Aug 26;351(9):940-1. — View Citation

Patrick DL, Burke LB, Powers JH, Scott JA, Rock EP, Dawisha S, O'Neill R, Kennedy DL. Patient-reported outcomes to support medical product labeling claims: FDA perspective. Value Health. 2007 Nov-Dec;10 Suppl 2:S125-37. Review. — View Citation

Straumann A, Simon HU. Eosinophilic esophagitis: escalating epidemiology? J Allergy Clin Immunol. 2005 Feb;115(2):418-9. — View Citation

Straumann A, Spichtin HP, Grize L, Bucher KA, Beglinger C, Simon HU. Natural history of primary eosinophilic esophagitis: a follow-up of 30 adult patients for up to 11.5 years. Gastroenterology. 2003 Dec;125(6):1660-9. — View Citation

U.S. Department of Health and Human Services FDA Center for Drug Evaluation and Research; U.S. Department of Health and Human Services FDA Center for Biologics Evaluation and Research; U.S. Department of Health and Human Services FDA Center for Devices and Radiological Health. Guidance for industry: patient-reported outcome measures: use in medical product development to support labeling claims: draft guidance. Health Qual Life Outcomes. 2006 Oct 11;4:79. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Development of an EE Activity Index 12 months No
Secondary Evaluation and validation of the activity index 2 years No
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