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Diagnosis of Acid Reflux Disease Using Novel Imaging: A Prospective Study

Primary Purpose

Non-erosive Reflux Disease

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Esomeprazole
Placebo
Sponsored by
Midwest Biomedical Research Foundation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Non-erosive Reflux Disease focused on measuring Non-erosive Reflux Disease

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 18 years of age
  • Capable of giving informed consents.
  • Cases of NERD will be recruited on the basis of presence of heartburn and/or regurgitation using two validated GERD questionnaires in conjunction with an abnormal esophageal pH result and absence of erosions at standard endoscopy.
  • Control subjects will include patients referred for an upper endoscopy for evaluation of non-reflux symptoms such as iron deficiency anemia, heme positive stools, screening of esophageal varices amongst others. A negative esophageal pH result and absence of erosions will be inclusion criteria for these patients.

Exclusion Criteria:

  • Presence of macroscopic erosive esophagitis
  • Pregnancy/lactation
  • Chronic anticoagulation
  • Patients with significant medical comorbidities (oxygen dependent chronic obstructive pulmonary disease, NYHA class III or IV congestive heart failure, recent diagnosis of cancer with a life-expectancy < 5 years)
  • History of Barrett's esophagus
  • Presence of columnar lined distal esophagus on endoscopy with intestinal metaplasia
  • Presence of cancer or mass lesion in the esophagus or stomach
  • Esophageal strictures
  • Peptic ulcer disease and Helicobacter pylori infection
  • Prior history of esophageal surgery
  • Allergic to PPIs
  • Patients on drugs known to cause pill-related esophagitis (e.g. potassium supplements)
  • Patients with HIV or other immunocompromised conditions who may have infectious esophagitis
  • Eosinophilic esophagitis

Sites / Locations

  • Department of Veterans Affairs Medical Center
  • Queen Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Esomeprazole

Placebo

Arm Description

proton pump inhibitor

placebo

Outcomes

Primary Outcome Measures

NBI endoscopy identifies changes in the distal esophagus that are specific for diagnosing patients with Non-Esophageal Reflux Disease.
Proportion of patients with NBI abnormalities in the NERD group vs. controls. Proportion of patients with resolution of NBI abnormalities after PPI therapy.

Secondary Outcome Measures

Full Information

First Posted
April 6, 2012
Last Updated
March 15, 2023
Sponsor
Midwest Biomedical Research Foundation
Collaborators
Kansas City Veteran Affairs Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02081404
Brief Title
Diagnosis of Acid Reflux Disease Using Novel Imaging: A Prospective Study
Official Title
Diagnosis of Acid Reflux Disease Using Novel Imaging: A Prospective Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
March 1, 2009 (Actual)
Primary Completion Date
January 5, 2020 (Actual)
Study Completion Date
August 5, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Midwest Biomedical Research Foundation
Collaborators
Kansas City Veteran Affairs Medical Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Gastroesophageal reflux disease (GERD), a common chronic disorder in the veteran population, is associated with drug costs exceeding $ 10 billion/year. Only 30-40% of patients with reflux symptoms have erosive esophagitis. The vast majority suffers from non erosive reflux disease (NERD), a condition in which standard endoscopy fails to identify any mucosal breaks and is unable to confirm the diagnosis. Unfortunately, a gold standard for the diagnosis of NERD does not exist. Narrow band imaging (NBI) utilizes spectral narrow band filters (incorporated into standard endoscopes) and helps to see abnormal areas not identified during standard endoscopy. Preliminary results have shown that NBI endoscopy may represent a significant improvement over standard endoscopy for the diagnosis of NERD. The purpose of this study is to accurately diagnosis non acid reflux disease by using a blue light (also known as NBI)upper endoscopy technique.
Detailed Description
Gastroesophageal reflux disease (GERD), a common chronic disorder in the veteran population, is associated with drug costs exceeding $ 10 billion/year. Only 30-40% of patients with reflux symptoms have erosive esophagitis. The vast majority suffers from NERD; a condition in which standard endoscopy fails to identify any mucosal breaks and is unable to confirm the diagnosis. Unfortunately, a gold standard for the diagnosis of NERD does not exist. 24-hour esophageal pH monitoring and histologic esophageal mucosal changes in NERD patients have limited accuracy to be routinely used in clinical practice. Narrow band imaging (NBI) utilizes spectral narrow band filters (incorporated into standard endoscopes) and enables imaging of features such as intrapapillary capillary loops (IPCLs); features not identified during standard endoscopy. Preliminary results have shown that NBI endoscopy may represent a significant improvement over standard endoscopy for the diagnosis of NERD. Our hypothesis is that NBI identifies changes in the distal esophagus that are specific for diagnosing patients with NERD. Specific Aim #1: To compare NBI features in the distal esophagus in patients with NERD (cases) and controls. Specific Aim #2: To determine whether the NBI features in NERD patients resolve after PPI therapy. Specific Aim #3: To correlate NBI findings with esophageal histology. Specific Aim #4: To assess the intra- and interobserver agreement for recognition of the proposed criteria for diagnosing NERD. Cases will be defined as patients with reflux symptoms (assessed by two validated questionnaires) with absent macroscopic erosions and abnormal esophageal pH results (NERD group). Control subjects will include patients with no reflux symptoms, absent macroscopic erosions and a normal esophageal pH result. To identify NBI findings as predictors of response, response to therapy in cases randomized to the PPI arm will be assessed using a validated GERD questionnaire and correlated with IPCL number and presence of microerosion. In addition, NBI findings in patients with reflux symptoms, no macroscopic erosions and normal esophageal pH result will also be compared with controls. Two biopsies will be obtained from the distal esophagus along with digital images and videorecordings. Statistical analysis will be done as follows: Aim 1 - chi-square and t-test; with logistic regression and calculation of odds ratios, Aim 2- McNemar's test and kappa statistic, Aim 3- Spearman's correlation coefficient and Aim 4- intraclass correlation coefficient. Potential impact on Health Care: GERD is common among patients and by obviating the need for additional investigations and reducing unnecessary drug costs, NBI endoscopy could have a considerable positive impact on patients with NERD. VA Project

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-erosive Reflux Disease
Keywords
Non-erosive Reflux Disease

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
Participant
Allocation
Randomized
Enrollment
98 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Esomeprazole
Arm Type
Active Comparator
Arm Description
proton pump inhibitor
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
placebo
Intervention Type
Drug
Intervention Name(s)
Esomeprazole
Other Intervention Name(s)
Nexium
Intervention Description
standard dose of proton pump inhibitor by mouth once a day for 30 days
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
inactive substance
Intervention Description
placebo
Primary Outcome Measure Information:
Title
NBI endoscopy identifies changes in the distal esophagus that are specific for diagnosing patients with Non-Esophageal Reflux Disease.
Description
Proportion of patients with NBI abnormalities in the NERD group vs. controls. Proportion of patients with resolution of NBI abnormalities after PPI therapy.
Time Frame
10 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18 years of age Capable of giving informed consents. Cases of NERD will be recruited on the basis of presence of heartburn and/or regurgitation using two validated GERD questionnaires in conjunction with an abnormal esophageal pH result and absence of erosions at standard endoscopy. Control subjects will include patients referred for an upper endoscopy for evaluation of non-reflux symptoms such as iron deficiency anemia, heme positive stools, screening of esophageal varices amongst others. A negative esophageal pH result and absence of erosions will be inclusion criteria for these patients. Exclusion Criteria: Presence of macroscopic erosive esophagitis Pregnancy/lactation Chronic anticoagulation Patients with significant medical comorbidities (oxygen dependent chronic obstructive pulmonary disease, NYHA class III or IV congestive heart failure, recent diagnosis of cancer with a life-expectancy < 5 years) History of Barrett's esophagus Presence of columnar lined distal esophagus on endoscopy with intestinal metaplasia Presence of cancer or mass lesion in the esophagus or stomach Esophageal strictures Peptic ulcer disease and Helicobacter pylori infection Prior history of esophageal surgery Allergic to PPIs Patients on drugs known to cause pill-related esophagitis (e.g. potassium supplements) Patients with HIV or other immunocompromised conditions who may have infectious esophagitis Eosinophilic esophagitis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Prateek Sharma, M.D.
Organizational Affiliation
VA Office of Research and Development
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Veterans Affairs Medical Center
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64128
Country
United States
Facility Name
Queen Medical Center
City
Nottingham
ZIP/Postal Code
NG7 2UH
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Participants individual participant data collected in the study will be available to other researchers upon request. Participants will be identified by participant number, age, race and gender. This information will be available at the end of the study and may be requested via email to april.higbee@va.gov.
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Diagnosis of Acid Reflux Disease Using Novel Imaging: A Prospective Study

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