Ablation of Esophageal Inlet Patches in Patients Referred for Bravo pH-Testing
Primary Purpose
GERD, Cough, Metaplasia
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Endoscopic ablation of inlet patch
Sponsored by
About this trial
This is an interventional treatment trial for GERD
Eligibility Criteria
Inclusion Criteria:
- Adult patients (age 18 and above)
- Referred for pH-testing for evaluation of possible extraesophageal-GERD
- Prior upper endoscopy performed
- Prior trial of PPI with an inadequate response
Exclusion Criteria:
- Patients who do not give consent
- Patients with abnormalities on their prior endoscopy including a significant hiatal hernia (>3 cm) or significant erosive esophagitis (Los Angeles class B or greater)
- Patients who did not fail a prior trial of PPI therapy
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Inlet patch
Controls
Arm Description
Patients found to have an inlet patch on upper endoscopy
Patients without an inlet patch on upper endoscopy
Outcomes
Primary Outcome Measures
Symptoms 6 months after procedure
The overall symptoms score
Secondary Outcome Measures
Symptoms 2 months after procedure
The overall symptoms score
Full Information
NCT ID
NCT05131932
First Posted
November 16, 2021
Last Updated
November 16, 2021
Sponsor
Assaf-Harofeh Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT05131932
Brief Title
Ablation of Esophageal Inlet Patches in Patients Referred for Bravo pH-Testing
Official Title
Ablation of Esophageal Inlet Patches in Patients Referred for pH-Testing Due to Possible Extra-Esophageal Symptoms of Gastro-Esophageal Reflux Disease
Study Type
Interventional
2. Study Status
Record Verification Date
November 2021
Overall Recruitment Status
Not yet recruiting
Study Start Date
December 2021 (Anticipated)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assaf-Harofeh Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Patients with suspected extra-esophageal manifestations of gastro-esophageal reflux disease (GERD), such as cough, hoarseness, and globus, are often referred for pH testing. However, many of these symptoms may actually be due to an esophageal inlet patch. We aim to evaluate patients referred for pH testing to see if they have an inlet patch, to perform ablation of the inlet patch if detected, and then compare the outcomes of patients with an inlet patch who underwent ablation versus those without an inlet patch.
Detailed Description
Background The diagnosis of gastro-esophageal reflux disease (GERD) is difficult when patients present with extra-esophageal symptoms such as chronic cough, frequent throat clearing, globus sensation, sore throat, and hoarseness, as opposed to the traditional symptoms of heartburn and regurgitation.[1-4] These patients are often given a trial of proton pump inhibitors (PPIs) to see if their symptoms improve. They often undergo an upper endoscopy, which is usually unrevealing,[5] and they may be evaluated by other specialties such as otolaryngology and pulmonology. Eventually, some of these patients are referred for esophageal pH-testing to evaluate for objective evidence of acid reflux.
The symptoms of extra-esophageal GERD (EE-GERD) are not specific for GERD and many of them overlap with the symptoms from inlet patches, also known as heterotopic gastric mucosa.[6-7] Inlet patches consist of small areas of gastric mucosa in the upper esophagus that are capable of producing acid.[8-10] Studies in which inlet patches are endoscopically ablated have shown improvement in several extra-esophageal symptoms including globus sensation, sore throat, and cough.[11-15] As inlet patches are notoriously overlooked on upper endoscopy[16] and can cause many of the same symptoms as EE-GERD, we suspect that they may be responsible for the symptoms in some patients who are referred for pH-testing due to suspected EE-GERD. We believe that a careful inspection of the upper esophagus will reveal inlet patches that were missed on initial endoscopy and that ablation of these inlet patches will help improve the patients' symptoms more than the standard treatment for EE-GERD.
Aims The primary aim of this study is to evaluate the improvement in symptoms of patients referred for pH-testing for suspected EE-GERD that are treated with endoscopic ablation of an inlet patch versus those who receive standard PPI therapy. Secondarily, we seek to determine the prevalence of inlet patches in these patients with reportedly normal endoscopies, as well as percentage of patients in this group with a positive pH study.
Methods Patients referred for pH-testing due to symptoms of possible EE-GERD will be evaluated. These patients will have their prior medical history reviewed. Those with a prior normal endoscopy and inadequate response to PPI therapy will be included.
Patients' symptoms will be assessed via a questionnaire across 8 domains including 6 symptoms of possible EE-GERD and 2 subjective scores of how the symptoms are affecting their lives (see Questionnaire below). A visual Likert scale from 0 to 10 will be used. An overall symptom score will be calculated based on the results of the 8 individual domains.
Patients will then undergo an upper endoscopy. During the endoscopy, care will be taken to assess for possible inlet patches. Advanced imaging techniques such as i-scan imaging will be used to aid in the detection of inlet patches. If one or more inlet patches are found, the number, size, and shape will be recorded, and it will be biopsied for histological confirmation. The inlet patch will then be ablated via the use of argon plasma coagulation (APC) as has been performed in prior studies.[11-13] During the endoscopy, a Bravo pH capsule will also be placed per standard protocol to complete a 48-hour pH study. The Bravo data will be interpreted according to standard procedure with a positive study defined as an elevated DeMeester score on either study day. All studies will be performed off of anti-acid medications such as PPIs.
The patients' symptoms will be re-assessed at 2 and 6 months following the endoscopy. This will be performed via telephone interviews with the patients completing the same symptom assessments as prior to the endoscopy. Changes in their medications and treatment as a result of the Bravo pH study results will also be evaluated.
The primary end point will be the symptom improvement in overall score in patients who underwent ablation of inlet patches versus those without inlet patches.
Inclusion Criteria
Adult patients (age 18 and above)
Referred for pH-testing for evaluation of possible EE-GERD
Prior upper endoscopy performed
Prior trial of PPI with an inadequate response Exclusion Criteria
Patients who do not give consent
Patients with abnormalities on their prior endoscopy including a significant hiatal hernia (>3 cm) or significant erosive esophagitis (Los Angeles class B or greater)
Patients who did not fail a prior trial of PPI therapy Anticipated number of subjects: 100
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
GERD, Cough, Metaplasia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Inlet patch
Arm Type
Experimental
Arm Description
Patients found to have an inlet patch on upper endoscopy
Arm Title
Controls
Arm Type
No Intervention
Arm Description
Patients without an inlet patch on upper endoscopy
Intervention Type
Procedure
Intervention Name(s)
Endoscopic ablation of inlet patch
Intervention Description
Endoscopic ablation of inlet patch using argon plasma coagulation (APC)
Primary Outcome Measure Information:
Title
Symptoms 6 months after procedure
Description
The overall symptoms score
Time Frame
6 months after procedure
Secondary Outcome Measure Information:
Title
Symptoms 2 months after procedure
Description
The overall symptoms score
Time Frame
2 months after procedure
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult patients (age 18 and above)
Referred for pH-testing for evaluation of possible extraesophageal-GERD
Prior upper endoscopy performed
Prior trial of PPI with an inadequate response
Exclusion Criteria:
Patients who do not give consent
Patients with abnormalities on their prior endoscopy including a significant hiatal hernia (>3 cm) or significant erosive esophagitis (Los Angeles class B or greater)
Patients who did not fail a prior trial of PPI therapy
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
IPD will be kept securely at the medical center
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Ablation of Esophageal Inlet Patches in Patients Referred for Bravo pH-Testing
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