search
Back to results

Endoscopic Cardiac Band Ligation for the Management of Refractory GERD After Laparoscopic Sleeve Gastrectomy (CLEAR)

Primary Purpose

GERD, Bariatric Surgery, Laparoscopic Sleeve Gastrectomy

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Cardia Band Ligation
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for GERD focused on measuring CLEAR, Antireflux procedure, LSG, GERD

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Obese patients who underwent surgical bariatric weight loss procedures with post-surgical GERD (LSG), not responding to once daily PPI therapy.
  • Obese patients who underwent surgical bariatric weight loss procedures with post-surgical GERD (LSG) who respond to maximum therapy with PPI + H2 blocker but are PPI averse or who refuse surgical therapy (conversion to RYGBP).
  • Patients older than 18 years and younger than 75 years of age at time of consent.
  • Patients able to provide written informed consent on the IRB/EC-approved informed consent form
  • Patients willing and able to comply with study requirements for follow-up

Exclusion Criteria:

  • Any patient with no prior surgical bariatric intervention.
  • Pre-existing esophageal stenosis/stricture preventing advancement of an endoscope during screening/baseline EGD.
  • Esophageal, gastric or duodenal malignancy.
  • Severe medical comorbidities precluding endoscopy, or limiting life expectancy to less than 2 years in the judgment of the endoscopist.
  • Uncontrolled coagulopathy or inability to be off anticoagulation or anti-platelet medication (ASA, Plavix) for 1 week prior to and 2 weeks after each endoscopy
  • Active fungal esophagitis, Grade C or D esophagitis.
  • Hiatal hernias > 2 cm or para-esophageal hernias.
  • Known portal hypertension, visible esophageal or gastric varices, or history of esophageal varices.
  • General poor health, multiple co-morbidities placing the patient at risk, or otherwise unsuitable for trial participation.
  • Pregnant or planning to become pregnant during period of study participation.
  • Patient refuses or is unable to provide written informed consent.
  • Prior surgical or endoscopic anti-reflux procedure.
  • Persistent dysphagia score greater than 0.
  • Vomiting more than once a week.
  • Biopsy-proven Barrett's esophagus.
  • HREM showing marked ineffective esophageal motility (defined by ≥ 5 weak or failed swallows per Chicago Classification v 3.0), esophagogastric outflow obstruction (EGJOO) or achalasia.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    CLEAR

    Arm Description

    Patients with GERD post LSG will undergo CLEAR (cardia band ligation).

    Outcomes

    Primary Outcome Measures

    Change in GERD-HQRL/RSI score
    Change in symptoms assessed by GERD-HQRL/RSI score at 6 months.
    Change in pH monitoring
    Change in objective pH monitoring at 6 months.

    Secondary Outcome Measures

    Mean change on the percentage of acid exposure time (% AET)
    Changes in acid exposure time from baseline.
    Safety of CLEAR procedure as assessed by treatment-related adverse events
    Assess overall safety (treatment-related adverse events) of CLEAR procedure defined by the ASGE-Lexicon classification.
    Rate of dysphagia post CLEAR
    Percentage of patients who develop dysphagia of any grade, associated with esophageal or gastric cardia stricture requiring dilation after CLEAR procedure.
    PPI discontinuation
    Percentage of patients who no longer require PPI at 6 months post CLEAR.
    PPI discontinuation
    Percentage of patients who no longer require PPI at 12 months post CLEAR.
    Treatment failure
    Defined as less than 50% improvement in GERD HQRL/RSI score or pH monitoring.

    Full Information

    First Posted
    February 23, 2021
    Last Updated
    September 22, 2021
    Sponsor
    Johns Hopkins University
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT04771247
    Brief Title
    Endoscopic Cardiac Band Ligation for the Management of Refractory GERD After Laparoscopic Sleeve Gastrectomy
    Acronym
    CLEAR
    Official Title
    Endoscopic Cardiac Band Ligation (CLEAR) Without Sleeve Stenosis for the Management of Refractory GERD After Laparoscopic Sleeve Gastrectomy (LSG)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2021
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    IRB approval withheld
    Study Start Date
    September 2021 (Anticipated)
    Primary Completion Date
    September 2021 (Anticipated)
    Study Completion Date
    September 2021 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Johns Hopkins University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    GERD is a prevalent condition worldwide, estimated to be around 20-30 % in North America. Obesity is rapidly increasing with an estimated prevalence of 66% in the adult population in the United States. Presently, bariatric interventions are the only sustainable method to address morbid obesity and its resulting comorbidities. One of the most common restrictive surgeries includes laparoscopic sleeve gastrectomy (LSG). Although very effective for treating obesity, some of these surgeries might cause deleterious effects regarding GERD, due to anatomical modifications. Refractory GERD is defined by lack of symptom control on maximum dose of PPI therapy. Cardia Band Ligation Anti-reflux (CLEAR) procedure utilizes multiple band ligations at the cardia in a 270-degree fashion, resulting in tissue necrosis and scar formation, narrowing the GE junction and enhancing the flap valve system. The investigators hypothesized that CLEAR can be a safe and efficient intervention to improve post bariatric GERD.
    Detailed Description
    GERD is a prevalent condition worldwide, estimated to be around 20-30 % in North America. Obesity is rapidly increasing with an estimated prevalence of 66% in the adult population in the United States. GERD symptoms are common in the obese population with data showing weekly GERD symptoms in 34.6% and erosive esophagitis 26.9% in people with BMI > 30 Kg/m^2. Reflux is associated with complications such as esophagitis, Barrett's Esophagus and ultimately esophageal adenocarcinoma. Presently, bariatric interventions are the only sustainable method to address morbid obesity and its resulting comorbidities. There are endoscopic and surgical bariatric interventions. Bariatric surgery has been shown to be an effective and efficient means of achieving significant weight loss in obese individuals. One of the most common restrictive surgeries includes laparoscopic sleeve gastrectomy (LSG). Although very effective for treating obesity, some of these surgeries might cause deleterious effects regarding GERD, due to anatomical modifications. LSG can increase the incidence of GERD, which may be explained from the changes in the angle of His and by increasing intragastric pressure. Pharmacological therapy with proton pump inhibitors (PPI), H2 blockers and lifestyle changes are first line forms of treatment utilized to control the symptoms related to GERD. However, patients who use pharmacological treatment experience reduction in quality of life and seek alternative options. Refractory GERD is defined by lack of symptom control on maximum dose of PPI therapy. Moreover, due to the anatomical changes associated with bariatric surgeries, the traditional surgical and endoscopic techniques (TIF, Nissen Fundoplication) used to treat GERD in the general population are not suitable for these patients. With the current trend of an increase of bariatric surgery and thus GERD that arises after these surgeries, new innovative techniques to treat GERD are needed, especially in PPI averse or non-responsive patients. Cardia Band Ligation Anti-reflux (CLEAR) procedure utilizes multiple band ligations at the cardia in a 270-degree fashion, resulting in tissue necrosis and scar formation, narrowing the GE junction and enhancing the flap valve system. The investigators will perform CLEAR by placing 4 bands at the GEJ. The investigators hypothesized that CLEAR can be a safe and efficient intervention to improve post bariatric GERD.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    GERD, Bariatric Surgery, Laparoscopic Sleeve Gastrectomy
    Keywords
    CLEAR, Antireflux procedure, LSG, GERD

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Model Description
    Prospective, single center, pilot clinical trial
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    CLEAR
    Arm Type
    Experimental
    Arm Description
    Patients with GERD post LSG will undergo CLEAR (cardia band ligation).
    Intervention Type
    Procedure
    Intervention Name(s)
    Cardia Band Ligation
    Intervention Description
    Patients will undergo cardia band ligation at the level of the GEJ.
    Primary Outcome Measure Information:
    Title
    Change in GERD-HQRL/RSI score
    Description
    Change in symptoms assessed by GERD-HQRL/RSI score at 6 months.
    Time Frame
    Baseline and 6 months
    Title
    Change in pH monitoring
    Description
    Change in objective pH monitoring at 6 months.
    Time Frame
    Baseline and 6 months
    Secondary Outcome Measure Information:
    Title
    Mean change on the percentage of acid exposure time (% AET)
    Description
    Changes in acid exposure time from baseline.
    Time Frame
    Baseline and 6 months
    Title
    Safety of CLEAR procedure as assessed by treatment-related adverse events
    Description
    Assess overall safety (treatment-related adverse events) of CLEAR procedure defined by the ASGE-Lexicon classification.
    Time Frame
    Up to 6 months
    Title
    Rate of dysphagia post CLEAR
    Description
    Percentage of patients who develop dysphagia of any grade, associated with esophageal or gastric cardia stricture requiring dilation after CLEAR procedure.
    Time Frame
    6-12 months
    Title
    PPI discontinuation
    Description
    Percentage of patients who no longer require PPI at 6 months post CLEAR.
    Time Frame
    6 months
    Title
    PPI discontinuation
    Description
    Percentage of patients who no longer require PPI at 12 months post CLEAR.
    Time Frame
    12 months
    Title
    Treatment failure
    Description
    Defined as less than 50% improvement in GERD HQRL/RSI score or pH monitoring.
    Time Frame
    6 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    75 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Obese patients who underwent surgical bariatric weight loss procedures with post-surgical GERD (LSG), not responding to once daily PPI therapy. Obese patients who underwent surgical bariatric weight loss procedures with post-surgical GERD (LSG) who respond to maximum therapy with PPI + H2 blocker but are PPI averse or who refuse surgical therapy (conversion to RYGBP). Patients older than 18 years and younger than 75 years of age at time of consent. Patients able to provide written informed consent on the IRB/EC-approved informed consent form Patients willing and able to comply with study requirements for follow-up Exclusion Criteria: Any patient with no prior surgical bariatric intervention. Pre-existing esophageal stenosis/stricture preventing advancement of an endoscope during screening/baseline EGD. Esophageal, gastric or duodenal malignancy. Severe medical comorbidities precluding endoscopy, or limiting life expectancy to less than 2 years in the judgment of the endoscopist. Uncontrolled coagulopathy or inability to be off anticoagulation or anti-platelet medication (ASA, Plavix) for 1 week prior to and 2 weeks after each endoscopy Active fungal esophagitis, Grade C or D esophagitis. Hiatal hernias > 2 cm or para-esophageal hernias. Known portal hypertension, visible esophageal or gastric varices, or history of esophageal varices. General poor health, multiple co-morbidities placing the patient at risk, or otherwise unsuitable for trial participation. Pregnant or planning to become pregnant during period of study participation. Patient refuses or is unable to provide written informed consent. Prior surgical or endoscopic anti-reflux procedure. Persistent dysphagia score greater than 0. Vomiting more than once a week. Biopsy-proven Barrett's esophagus. HREM showing marked ineffective esophageal motility (defined by ≥ 5 weak or failed swallows per Chicago Classification v 3.0), esophagogastric outflow obstruction (EGJOO) or achalasia.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Olaya I Brewer Gutierrez
    Organizational Affiliation
    Johns Hopkins University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    29488430
    Citation
    Seleem WM, Hanafy AS, Mohamed SI. Endoscopic management of refractory gastroesophageal reflux disease. Scand J Gastroenterol. 2018 Apr;53(4):390-397. doi: 10.1080/00365521.2018.1445775. Epub 2018 Feb 28.
    Results Reference
    background

    Learn more about this trial

    Endoscopic Cardiac Band Ligation for the Management of Refractory GERD After Laparoscopic Sleeve Gastrectomy

    We'll reach out to this number within 24 hrs