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Withdrawn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
About this trial
This is an interventional treatment trial for GERD focused on measuring CLEAR, Antireflux procedure, LSG, GERD
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.
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
NCT ID
NCT04771247
First Posted
February 23, 2021
Last Updated
September 22, 2021
Sponsor
Johns Hopkins University
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
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Endoscopic Cardiac Band Ligation for the Management of Refractory GERD After Laparoscopic Sleeve Gastrectomy
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