search
Back to results

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
Midwest Veterans' Biomedical Research Foundation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastro Esophageal Reflux

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
September 29, 2022
Last Updated
October 5, 2022
Sponsor
Midwest Veterans' Biomedical Research Foundation
search

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
Citations:
PubMed Identifier
9136821
Citation
Locke GR 3rd, Talley NJ, Fett SL, Zinsmeister AR, Melton LJ 3rd. Prevalence and clinical spectrum of gastroesophageal reflux: a population-based study in Olmsted County, Minnesota. Gastroenterology. 1997 May;112(5):1448-56. doi: 10.1016/s0016-5085(97)70025-8.
Results Reference
background
PubMed Identifier
23853213
Citation
El-Serag HB, Sweet S, Winchester CC, Dent J. Update on the epidemiology of gastro-oesophageal reflux disease: a systematic review. Gut. 2014 Jun;63(6):871-80. doi: 10.1136/gutjnl-2012-304269. Epub 2013 Jul 13.
Results Reference
background
PubMed Identifier
16061918
Citation
Hampel H, Abraham NS, El-Serag HB. Meta-analysis: obesity and the risk for gastroesophageal reflux disease and its complications. Ann Intern Med. 2005 Aug 2;143(3):199-211. doi: 10.7326/0003-4819-143-3-200508020-00006.
Results Reference
background
PubMed Identifier
29686276
Citation
Yadlapati R, Vaezi MF, Vela MF, Spechler SJ, Shaheen NJ, Richter J, Lacy BE, Katzka D, Katz PO, Kahrilas PJ, Gyawali PC, Gerson L, Fass R, Castell DO, Craft J, Hillman L, Pandolfino JE. Management options for patients with GERD and persistent symptoms on proton pump inhibitors: recommendations from an expert panel. Am J Gastroenterol. 2018 Jul;113(7):980-986. doi: 10.1038/s41395-018-0045-4. Epub 2018 Apr 24.
Results Reference
background
PubMed Identifier
31866243
Citation
Delshad SD, Almario CV, Chey WD, Spiegel BMR. Prevalence of Gastroesophageal Reflux Disease and Proton Pump Inhibitor-Refractory Symptoms. Gastroenterology. 2020 Apr;158(5):1250-1261.e2. doi: 10.1053/j.gastro.2019.12.014. Epub 2019 Dec 19.
Results Reference
background
PubMed Identifier
28528705
Citation
Vaezi MF, Yang YX, Howden CW. Complications of Proton Pump Inhibitor Therapy. Gastroenterology. 2017 Jul;153(1):35-48. doi: 10.1053/j.gastro.2017.04.047. Epub 2017 May 19.
Results Reference
background
PubMed Identifier
28898377
Citation
Maret-Ouda J, Wahlin K, El-Serag HB, Lagergren J. Association Between Laparoscopic Antireflux Surgery and Recurrence of Gastroesophageal Reflux. JAMA. 2017 Sep 12;318(10):939-946. doi: 10.1001/jama.2017.10981.
Results Reference
background
PubMed Identifier
25823768
Citation
Witteman BP, Conchillo JM, Rinsma NF, Betzel B, Peeters A, Koek GH, Stassen LP, Bouvy ND. Randomized controlled trial of transoral incisionless fundoplication vs. proton pump inhibitors for treatment of gastroesophageal reflux disease. Am J Gastroenterol. 2015 Apr;110(4):531-42. doi: 10.1038/ajg.2015.28. Epub 2015 Mar 31.
Results Reference
background
PubMed Identifier
28859357
Citation
Hillman L, Yadlapati R, Whitsett M, Thuluvath AJ, Berendsen MA, Pandolfino JE. Review of antireflux procedures for proton pump inhibitor nonresponsive gastroesophageal reflux disease. Dis Esophagus. 2017 Sep 1;30(9):1-14. doi: 10.1093/dote/dox054.
Results Reference
background
PubMed Identifier
32343977
Citation
Hernandez Mondragon OV, Zamarripa Mottu RA, Garcia Contreras LF, Gutierrez Aguilar RA, Solorzano Pineda OM, Blanco Velasco G, Murcio Perez E. Clinical feasibility of a new antireflux ablation therapy on gastroesophageal reflux disease (with video). Gastrointest Endosc. 2020 Dec;92(6):1190-1201. doi: 10.1016/j.gie.2020.04.046. Epub 2020 Apr 25.
Results Reference
background
PubMed Identifier
32010745
Citation
Inoue H, Tanabe M, de Santiago ER, Abad MRA, Shimamura Y, Fujiyoshi Y, Ueno A, Sumi K, Tomida H, Iwaya Y, Ikeda H, Onimaru M. Anti-reflux mucosal ablation (ARMA) as a new treatment for gastroesophageal reflux refractory to proton pump inhibitors: a pilot study. Endosc Int Open. 2020 Feb;8(2):E133-E138. doi: 10.1055/a-1031-9436. Epub 2020 Jan 22.
Results Reference
background
PubMed Identifier
11742159
Citation
Taieb S, Rolachon A, Cenni JC, Nancey S, Bonvoisin S, Descos L, Fournet J, Gerard JP, Flourie B. Effective use of argon plasma coagulation in the treatment of severe radiation proctitis. Dis Colon Rectum. 2001 Dec;44(12):1766-71. doi: 10.1007/BF02234452.
Results Reference
background
PubMed Identifier
24138285
Citation
Sami SS, Al-Araji SA, Ragunath K. Review article: gastrointestinal angiodysplasia - pathogenesis, diagnosis and management. Aliment Pharmacol Ther. 2014 Jan;39(1):15-34. doi: 10.1111/apt.12527. Epub 2013 Oct 20.
Results Reference
background
PubMed Identifier
30076843
Citation
Peerally MF, Bhandari P, Ragunath K, Barr H, Stokes C, Haidry R, Lovat L, Smart H, Harrison R, Smith K, Morris T, de Caestecker JS. Radiofrequency ablation compared with argon plasma coagulation after endoscopic resection of high-grade dysplasia or stage T1 adenocarcinoma in Barrett's esophagus: a randomized pilot study (BRIDE). Gastrointest Endosc. 2019 Apr;89(4):680-689. doi: 10.1016/j.gie.2018.07.031. Epub 2018 Aug 1.
Results Reference
background
PubMed Identifier
25360316
Citation
Manner H, Neugebauer A, Scharpf M, Braun K, May A, Ell C, Fend F, Enderle MD. The tissue effect of argon-plasma coagulation with prior submucosal injection (Hybrid-APC) versus standard APC: A randomized ex-vivo study. United European Gastroenterol J. 2014 Oct;2(5):383-90. doi: 10.1177/2050640614544315.
Results Reference
background
PubMed Identifier
25330784
Citation
Inoue H, Ito H, Ikeda H, Sato C, Sato H, Phalanusitthepha C, Hayee B, Eleftheriadis N, Kudo SE. Anti-reflux mucosectomy for gastroesophageal reflux disease in the absence of hiatus hernia: a pilot study. Ann Gastroenterol. 2014;27(4):346-351.
Results Reference
background
PubMed Identifier
26526815
Citation
Desjardin M, Luc G, Collet D, Zerbib F. 24-hour pH-impedance monitoring on therapy to select patients with refractory reflux symptoms for antireflux surgery. A single center retrospective study. Neurogastroenterol Motil. 2016 Jan;28(1):146-52. doi: 10.1111/nmo.12715. Epub 2015 Nov 3.
Results Reference
background
PubMed Identifier
31788546
Citation
Fayad L, Oberbach A, Schweitzer M, Askin F, Voltaggio L, Larman T, Enderle M, Hahn H, Khashab MA, Kalloo AN, Kumbhari V. Gastric mucosal devitalization (GMD): translation to a novel endoscopic metabolic therapy. Endosc Int Open. 2019 Dec;7(12):E1640-E1645. doi: 10.1055/a-0957-3067. Epub 2019 Nov 25.
Results Reference
background
PubMed Identifier
16928254
Citation
Vakil N, van Zanten SV, Kahrilas P, Dent J, Jones R; Global Consensus Group. The Montreal definition and classification of gastroesophageal reflux disease: a global evidence-based consensus. Am J Gastroenterol. 2006 Aug;101(8):1900-20; quiz 1943. doi: 10.1111/j.1572-0241.2006.00630.x.
Results Reference
result
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.

Learn more about this trial

Anti-Reflux Endoscopic TX Using APC (AREA) in GERD Patients: (The AREA Study)

We'll reach out to this number within 24 hrs