Anti-Reflux Endoscopic TX Using APC (AREA) in GERD Patients: (The AREA Study) (AREA21)
Primary Purpose
Gastro Esophageal Reflux
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
ARAT
Sham intervention (control)
Sponsored by
About this trial
This is an interventional treatment trial for Gastro Esophageal Reflux
Eligibility Criteria
Inclusion Criteria:
- Chronic GERD symptoms (at least 1 typical symptom of GERD, i.e. heartburn or acid reflux/regurgitation at least twice a week) for last 6 months
- Objective evidence of reflux disease (positive ambulatory pH study.)
Exclusion Criteria:
- Patients unable to or unwilling to participate or consent.
- Age <18 years or >80 years.
- Allergic or intolerant to PPI medications.
- Large hiatal hernia > 3 cm and Hill grade IV.
- Barrett's esophagus.
- Esophageal stricture with any prior intervention.
- Major motility disorder.
- Eosinophilic esophagitis.
- Gastroparesis documented by abnormal gastric emptying time.
- Previous fundoplication, myotomy or LINX surgery.
- Cirrhosis with esophageal and/or gastric varices.
Sites / Locations
- Kansas City VA HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Sham Comparator
Arm Label
Anti-reflux mucosal ablation (ARAT)
No treatment
Arm Description
ablation in the gastric cardia using hybrid argon plasma coagulation
no ablation
Outcomes
Primary Outcome Measures
Change in GERD health related quality of life (GERD-HRQL) score
The primary outcome of quality of life will be measured using the validated GERD related quality of life questionnaire (GERD-HRQL). The total score is 50, and a higher score is associated with more severe symptoms.
Secondary Outcome Measures
Change in Reflux disease questionnaire (RDQ) score
RDQ scores will be assessed using a validated questionnaire scale. The total score is 40, and a higher score is associated with more severe symptoms.
Change in Proton pump inhibitor (PPI) use
Frequency of PPI medication use
Acid exposure time (AET)
Ambulatory acid reflux testing (wireless pH monitoring system) for measurement. Acid exposure time measures amount of time spent in pH <4. A time >4% is considered positive for acid reflux.
Adverse events
Frequency of any adverse event including chest pain, bleeding, dysphagia, hospitalization
Change in Hiatal hernia grading
Hill grade for hiatal hernia assessment during endoscopy. There are 4 grades: I, II, III and IV depending on the appearance of the hiatus on endoscopy.
Esophagitis incidence
LA grade esophagitis at the time of endoscopy
Full Information
NCT ID
NCT05570448
First Posted
September 29, 2022
Last Updated
October 5, 2022
Sponsor
Midwest Veterans' Biomedical Research Foundation
1. Study Identification
Unique Protocol Identification Number
NCT05570448
Brief Title
Anti-Reflux Endoscopic TX Using APC (AREA) in GERD Patients: (The AREA Study)
Acronym
AREA21
Official Title
Anti-Reflux Endoscopic Therapy Using Argon Plasma Coagulation (AREA) in Gastroesophageal Reflux Disease (GERD) Patients: A Single Center, Randomized, Sham, Controlled Trial (The AREA Study)
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 15, 2022 (Actual)
Primary Completion Date
February 2025 (Anticipated)
Study Completion Date
April 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Midwest Veterans' Biomedical Research Foundation
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This will be a randomized clinical trial examining the efficacy and safety of ARAT (intervention group) in patients with chronic GERD symptoms (typical symptoms of GERD, i.e. heartburn or acid reflux/regurgitation at least twice a week) for the last 6 months.
Patients must have a positive pH test and a negative manometry (no treatment) procedure.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastro Esophageal Reflux
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
36 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Anti-reflux mucosal ablation (ARAT)
Arm Type
Active Comparator
Arm Description
ablation in the gastric cardia using hybrid argon plasma coagulation
Arm Title
No treatment
Arm Type
Sham Comparator
Arm Description
no ablation
Intervention Type
Procedure
Intervention Name(s)
ARAT
Other Intervention Name(s)
Anti-reflux mucosal ablation
Intervention Description
For patients randomized to ARAT intervention, the area of cardia, along greater curvature will be cleaned followed by demarcation of a 1-1.5 cm area of non-ablation zone with two vertical lines by use of Pulsed APC (30W, Effect 2) using the H-APC catheter. Next, the area of cardia, on either side will be injected in sequence using a methylene blue (0.5%) and normal saline (0.9%) using the H-APC catheter jet system (Effect 30-70). Next, the mucosa, starting below the z-line and up to 3 cm below will be treated by Pulsed APC 50W-80W till golden-brown discoloration of the ablated tissue in 270-320 degree. For patients randomized to control or sham intervention, upper endoscopy with procedural sedation was performed followed by markings of landmarks followed by gastroscope retroflexion in the gastric cardia with at least 15 minute of examination time. No H-APC or submucosal injection or other intervention will be performed.
Intervention Type
Procedure
Intervention Name(s)
Sham intervention (control)
Intervention Description
Patients randomized to the control arm, will undergo a sham intervention. This will include performing upper endoscopy with procedural sedation followed by markings of landmarks as described. This will be followed by gastroscope retroflexion in the gastric cardia with at least 15 minute of examination time spent in retroflexion to reciprocate the H-APC intervention. No H-APC or submucosal injection or other intervention will be performed during the upper endoscopy with sham intervention. All Patients will also continue their PPI daily for 4 weeks.
Primary Outcome Measure Information:
Title
Change in GERD health related quality of life (GERD-HRQL) score
Description
The primary outcome of quality of life will be measured using the validated GERD related quality of life questionnaire (GERD-HRQL). The total score is 50, and a higher score is associated with more severe symptoms.
Time Frame
At 3, 6 and 12 months
Secondary Outcome Measure Information:
Title
Change in Reflux disease questionnaire (RDQ) score
Description
RDQ scores will be assessed using a validated questionnaire scale. The total score is 40, and a higher score is associated with more severe symptoms.
Time Frame
At 3, 6 and 12 months
Title
Change in Proton pump inhibitor (PPI) use
Description
Frequency of PPI medication use
Time Frame
At 3, 6 and 12 months
Title
Acid exposure time (AET)
Description
Ambulatory acid reflux testing (wireless pH monitoring system) for measurement. Acid exposure time measures amount of time spent in pH <4. A time >4% is considered positive for acid reflux.
Time Frame
At 3 and 12 months
Title
Adverse events
Description
Frequency of any adverse event including chest pain, bleeding, dysphagia, hospitalization
Time Frame
Post-randomization (Day 1, Day 30, 3rd, 6th and 12th month)
Title
Change in Hiatal hernia grading
Description
Hill grade for hiatal hernia assessment during endoscopy. There are 4 grades: I, II, III and IV depending on the appearance of the hiatus on endoscopy.
Time Frame
At 3 and 12 months
Title
Esophagitis incidence
Description
LA grade esophagitis at the time of endoscopy
Time Frame
At 3 and 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Chronic GERD symptoms (at least 1 typical symptom of GERD, i.e. heartburn or acid reflux/regurgitation at least twice a week) for last 6 months
Objective evidence of reflux disease (positive ambulatory pH study.)
Exclusion Criteria:
Patients unable to or unwilling to participate or consent.
Age <18 years or >80 years.
Allergic or intolerant to PPI medications.
Large hiatal hernia > 3 cm and Hill grade IV.
Barrett's esophagus.
Esophageal stricture with any prior intervention.
Major motility disorder.
Eosinophilic esophagitis.
Gastroparesis documented by abnormal gastric emptying time.
Previous fundoplication, myotomy or LINX surgery.
Cirrhosis with esophageal and/or gastric varices.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
April Higbee, BSN
Phone
816-861-4700
Email
april.higbee@va.gov
First Name & Middle Initial & Last Name or Official Title & Degree
Carlissa Campbell, MS
Phone
816-861-4700
Email
Carlissa.Campbell@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Prateek Sharma, MD
Organizational Affiliation
Kansas City VA Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Madhav Desai, MD
Organizational Affiliation
Kansas City VA Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Kansas City VA Hospital
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64128
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
April Higbee, BSN
Phone
816-861-4700
Email
April.Higbee@va.gov
First Name & Middle Initial & Last Name & Degree
Carlissa Campbell, MA
Phone
816-861-4700
Email
Carlissa.Campbell@va.gov
First Name & Middle Initial & Last Name & Degree
Prateek Sharma, MD
First Name & Middle Initial & Last Name & Degree
Madhav Desai, MD
First Name & Middle Initial & Last Name & Degree
Abhilash Perisetti, MD
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Links:
URL
https://www.semanticscholar.org/paper/Anti-Reflux-Mucosal-Ablation-(ARMA)-For-Refractory-Kalapala-Jagtap/744a295131bedf263ba6f4c13126d0c5afc93b14
Description
, Kalapala R, Nabi Z, et al. Anti-Reflux Mucosal Ablation (ARMA) For Refractory Gastroesophageal Reflux Disease - An Interim Analysis, 2021.
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Anti-Reflux Endoscopic TX Using APC (AREA) in GERD Patients: (The AREA Study)
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