- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00219492
Role of Esophageal Mast Cell Activation in Noncardiac Chest Pain (NCCP)
June 16, 2017 updated by: Milton S. Hershey Medical Center
Chest pain is a common clinical complaint.
About 30% patients with chest pain will have a normal coronary angiogram and are described as having noncardiac chest pain (NCCP).
It is estimated that 25% of the population complain of chest pain at some time in their lifetime.
The pathogenesis of NCCP is unknown.
Esophageal hypersensitivity as a result of inflammation is considered to be an important mechanism in the development of this pain sensation.
Little is currently known about the interaction between inflammatory mediators and peripheral afferent nerve terminals in the esophagus.
The mast cell is one of the most enriched pro-inflammatory cells in the gastrointestinal tract.
Activation of the mucosal mast cell releases a variety of mediators into adjacent tissues.
We hypothesize that mediators released by mast cells sensitize esophageal nociceptors and induce pain sensation.
Study Overview
Status
Completed
Conditions
Detailed Description
- Key Objectives: To determine the density and activation of esophageal mast cells in non-cardiac chest pain patients. We expect to find mast cell activation, as measured by mast cell count or degranluation, tryptase staining, and histamine release, will be greater in NCCP patients compared to controls, and the increased mast cell activation will correlate with the severity of NCCP. These results will expand our understanding of the pathogenesis of esophageal originated NCCP, and allow the development of new diagnostic and treatment options.
- Study Population: (i) NCCP (ii) Reflux esophagitis (iii) Control subjects.
- Summary of Procedures: (i) symptom assessment by chest pain questionnaire; (ii) esophageal reflux evaluation by review of records of 24-hour pH monitoring; (iii) evidence of esophagitis by endoscopy; (iv) esophageal biopsy by endoscopy; (v) mast cell activation study in biopsy specimen by mast cell count, tryptase and Transient receptor potential vanniloid-1 (TRPV1) staining, and histamine release assay.
- Major Risks & Discomforts: There are no major risks & discomforts other than involved in standard upper GI endoscopy.
Study Type
Observational
Enrollment (Actual)
86
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Pennsylvania
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Hershey, Pennsylvania, United States, 17033
- Penn State College of Medicine Hershey Medical Center
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 70 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- NCCP - presence of a history of chest pain with a negative cardiac evaluation, no evidence of gross esophagitis on endoscopy, and lack of any exclusion criteria; Reflux esophagitis - presence of chest pain or heartburn, negative cardiac evaluation, lack of exclusion criteria and presence of esophagitis on endoscopy;
- Controls - lack of history of chest pain, lack of exclusion criteria and lack of esophagitis on endoscopy. It is anticipated that patients being evaluated for heme positive stool or GI bleeding would be included as controls.
Exclusion Criteria:
- History of ischemic heart disease, history of asthma, significant food allergies, celiac disease, chronic inflammatory conditions (SLE, rheumatoid arthritis), atopic skin disease, varices, coagulopathy, recent drug treatment with steroids.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Shaoyong Yu, MD, MPH, Department of Medicine, Penn State College of Medicine Hershey Medical Center
- Study Director: Ann Ouyang, MD, Penn State College of Medicine Hershey Medical Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2005
Primary Completion (Actual)
August 21, 2014
Study Completion (Actual)
August 21, 2014
Study Registration Dates
First Submitted
September 16, 2005
First Submitted That Met QC Criteria
September 16, 2005
First Posted (Estimate)
September 22, 2005
Study Record Updates
Last Update Posted (Actual)
June 20, 2017
Last Update Submitted That Met QC Criteria
June 16, 2017
Last Verified
June 1, 2017
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 21370
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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