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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
Assaf-Harofeh Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for GERD

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    November 16, 2021
    Last Updated
    November 16, 2021
    Sponsor
    Assaf-Harofeh Medical Center
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    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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