CENERDD: Confocal Endomicroscopy for Non-Erosive Reflux Disease Detection
Study Details
Study Description
Brief Summary
Primary Objective:
Evaluate response to NERD treatment between patients with normal endomicroscopy findings compared with patients with abnormal endomicroscopy findings.
Secondary Objectives:
To evaluate the role of probe based endomicroscopy in the diagnosis of NERD by evaluating dilated intercellular spaces, evaluation of IPCL, and quantification of fluorescein leak.
Quality of life at study entry and end of study. Compare two medications under study within each group as a subgroup analysis.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
The purpose of this study is to evaluate response to non-erosive reflux disease (NERD) treatment between patients with normal endomicroscopy findings compared with patients with abnormal endomicroscopy findings. The researchers will compare two different drug regimens for the NERD subjects to evaluate their effectiveness in reducing NERD-related symptoms. In addition, the researchers will be testing the function and effectiveness of the confocal endomicroscopy procedure to be used during the study. Researchers will be continuing to assess the status, symptoms, and any changes associated with the symptoms subjects are experiencing.
The confocal endomicroscopy procedure utilizes a powerful microscope that is used during an endoscopy. An endoscopy is a procedure that allows us to scope/view the inside of the esophagus and stomach using a camera in precise detail.
An endoscopy procedure and measurements of acid in the esophagus have been used to determine if the investigators think acid is causing the symptoms. Traditionally, acid blocking medications called proton pump inhibitors (PPIs such as Esomeprazole, Lansoprazole, Omeprazole, and Pantoprazole), or medications such as Sucralfate have been used to treat the symptoms of NERD.
The medical community believes that these symptoms are due to increased spaces between the cells that make up the esophagus. They can directly see those spaces using the confocal endomicroscopy.
Patients are asked to participate in this study if they are 18 years of age or older and have typical symptoms for patients diagnosed with NERD that have not responded to the first attempted medication.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Other: Proton Pump Inhibitor (PPI) Therapy 2x daily Proton Pump Inhibitor (PPI) Therapy for 8 weeks |
Drug: Proton Pump Inhibitor (PPI) Therapy
Subject will take a proton pump inhibitor (PPI) of their choice (Omeprazole, Esomeprazole, Pantoprazole, or Lansoprazole) 2 times a day for 8 weeks.
Other Names:
|
| Other: Sucralfate 4x daily Sucralfate slurry, 1g, for 8 weeks |
Drug: Sucralfate
Subject will take Sucralfate 4 times a day for 8 weeks.
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Evaluate non erosive reflux disease (NERD) Symptoms. [20 weeks]
Reflux Disease Questionnaire (RDQ)
Secondary Outcome Measures
- Evaluate the role of probe based endomicroscopy in the diagnosis of NERD by evaluating dilated intercellular spaces, evaluation of IPCL, and quantification of fluorescein leak. [20 weeks]
A 3 minute video recording of microscopic images starting with the injection of the fluorescein will be captured during the time of endoscopy. The goal is also to see if the time to seeing fluorescein in the intracellular spaces correlates with a diagnosis of NERD. Time, measured in seconds, to first visualization of intrapapillary loops and intercellular gaps and fluorescein leak will be obtained and assess by trained endoscopists.
- Compare quality of life in patients with NERD. [20 weeks]
Quality of life questionnaire (SF-36)
- Compare two medications within each NERD study groups as a subgroup analysis. [20 weeks]
Categorical and binary demographics and outcomes will be assessed through a likelihood-ratio chi square test or a Fischer's exact test.Continuous outcomes, including time to fluorescein intracellular, will be assessed through a Student's t test or Wilcoxon rank sum, if the distribution of particular continuous variables is non-normal, tested through a Shapiro-Wilk statistic. Statistical significance will be determined at p values less than 0.05.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Individuals older than 18 years who score a 12 or greater on the Reflux Disease Questionnaire and have failed a four week trial of daily proton pump inhibitor.
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Subjects without gastroesophageal reflux disease (GERD) undergoing upper endomicroscopy for other indications will be recruited into study as controls.
Exclusion Criteria:
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Barrett's esophagus
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Use of twice daily proton pump inhibitor within 4 weeks of study entry
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Esophageal varices
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Coagulopathy (aspirin, NSAIDS and Plavix are allowed. Coumadin, Xarelto, heparin are not allowed.)
-
Gastrointestinal cancer or mass
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Previous surgery involving the esophagus, stomach or duodenum
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Pregnancy
-
Allergy to either sucralfate or proton pump inhibitors
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Touro Infirmary New Orleans | New Orleans | Louisiana | United States | 70112 |
| 2 | University Medical Center New Orleans | New Orleans | Louisiana | United States | 70112 |
Sponsors and Collaborators
- LCMC Health
Investigators
- Principal Investigator: Virendra Joshi, MD, LCMC Health
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- CENERDD