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A Randomized Controlled Trial of Laparoscopic Nissen Fundoplication Treatment of Patients With Chronic GERD

Primary Purpose

Gastroesophageal Reflux

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Proton Pump Inhibitors
Laparoscopic Nissen Fundoplication
Sponsored by
McMaster University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastroesophageal Reflux

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Male and female GERD patients aged 18-70 years with GERD symptoms. Prior long-term treatment with PPI with minimum duration of 1 year with expected future duration of at least 2 more years. Controlled on 20-40mg/day maintenance PPI therapy prior to study, defined as GERD symptom score<18 and score of 70 or more on 1-100 Global Rating Scale at screening (on medication). Increase in GERD symptom score>=15 points at baseline (off omeprazole). GERD symptom score>=18 at baseline (off omeprazole). Percent acid reflux in 24hr 4% at baseline (off omeprazole). Positive Bernstein test at baseline. Willingness to adhere to randomized treatment with availability for 3 years of follow-up. Ability to answer self and interviewer-administered questions in English. Signed informed consent. Exclusion Criteria: Aperistaltic esophagus. Severe cardiac, respiratory, hematologic or other disease constituting an unacceptable surgical risk in the investigator's opinion. Previous gastric, esophageal or anti-reflux surgery. History of malignancy within the last year with the exception of basal cell carcinoma. Pregnancy or an intention to become pregnant in the following year.

Sites / Locations

  • St. Joseph's Healthcare Hamilton

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Proton Pump Inhibitor

Laparoscopic Nissen Fundoplication

Arm Description

Patients randomized to medical therapy received optimized treatment with PPI using a standardized management protocol based on best evidence and published guidelines.

Surgical patients underwent LNF using previously published technique.

Outcomes

Primary Outcome Measures

GERD Symptom Scale
Symptom-free Day Measurement
Cost Measurement

Secondary Outcome Measures

24-hour pH
Economic Analysis
Endoscopy
Esophageal manometry
Health related quality of life (SF-36)
Health Utility Index
Respiratory function, airways hypersensitivity and inflammation and microaspiration

Full Information

First Posted
September 12, 2005
Last Updated
November 14, 2012
Sponsor
McMaster University
Collaborators
St. Joseph's Healthcare Hamilton
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1. Study Identification

Unique Protocol Identification Number
NCT00182260
Brief Title
A Randomized Controlled Trial of Laparoscopic Nissen Fundoplication Treatment of Patients With Chronic GERD
Official Title
ELVIS (Esophagitis-Laparoscopy Versus Inhibitors of Secretion) A Randomized Controlled Trial of Laparoscopic Nissen Fundoplication (LNF) Versus Omeprazole for Treatment of Patients With Chronic Gastro-Esophageal Reflux Disease (GERD)
Study Type
Interventional

2. Study Status

Record Verification Date
November 2012
Overall Recruitment Status
Completed
Study Start Date
January 2000 (undefined)
Primary Completion Date
April 2010 (Actual)
Study Completion Date
April 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
McMaster University
Collaborators
St. Joseph's Healthcare Hamilton

4. Oversight

5. Study Description

Brief Summary
LNF is an effective intervention in the management of patients with chronic GERD requiring maintenance therapy. LNF is cost-effective compared with long-term medical therapy. LNF is more effective than maximum medical therapy in control of respiratory symptoms and complications of GERD.
Detailed Description
GERD encompasses a variety of symptoms and pathological findings caused by the reflux of gastric contents into the esophagus although symptoms and pathology may occur independently of each other. GERD usually presents with typical symptoms of retrosternal burning (heartburn) with or without chest pain and regurgitation of gastric contents into the back of the mouth. However, symptoms often occur in the absence of abnormalities associated with GERD, such as esophageal erosions, ulceration, stricturing or Barrett's esophagus. There is no clear correlation between symptoms and the histological features of GERD. Less prevalent manifestations of GERD include the geneses of dental erosions and respiratory disease including aspiration pneumonia, asthma, chronic laryngitis. Most often, GERD is due to excessive reflux of gastric contents into the esophagus rather than gastric acid hypersecretion. Reflux is caused by an increase in the frequency of inappropriate transient relaxations of the lower esophageal sphincter (LES). In most patients, basal resting LES pressure is normal although LES hypotonia, reduced esophageal body contractility and the presence of a hiatus hernia may exacerbate reflux or reduce esophageal clearance. Impaired esophageal mucosal resistance can increase the potential for esophageal damage. Bile acids and pancreatic enzymes have been implicated in the pathogenesis of GERD but it is generally accepted that the major causes of esophageal symptoms and injury are gastric acid and pepsin, which are active only at low ambient pH. Severity of esophagitis and of reflux symptoms correlate well with the duration of esophageal acid exposure with clear correlation between acid secretory inhibition and esophagitis healing rates for any given drug. On this basis, treatment for GERD has been directed towards: Minimization of potential precipitating factors by lifestyle modifications such as weight loss, small meals and, avoidance of alcohol and tobacco. Improving LES pressure, esophageal clearance and gastric emptying, using prokinetic agents. Neutralization of acid in the stomach or esophagus, using antacids. Reduction of acid secretion, using histamine receptor antagonists(H2RAs) or PPI's. Surgical prevention of gastro-esophageal reflux by fundoplication. In practice, the latter two approaches are the most successful for patients with more severe GERD and PPI's have proven more efficacious than H2RAs.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastroesophageal Reflux

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
216 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Proton Pump Inhibitor
Arm Type
Active Comparator
Arm Description
Patients randomized to medical therapy received optimized treatment with PPI using a standardized management protocol based on best evidence and published guidelines.
Arm Title
Laparoscopic Nissen Fundoplication
Arm Type
Active Comparator
Arm Description
Surgical patients underwent LNF using previously published technique.
Intervention Type
Drug
Intervention Name(s)
Proton Pump Inhibitors
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic Nissen Fundoplication
Primary Outcome Measure Information:
Title
GERD Symptom Scale
Title
Symptom-free Day Measurement
Title
Cost Measurement
Secondary Outcome Measure Information:
Title
24-hour pH
Title
Economic Analysis
Title
Endoscopy
Title
Esophageal manometry
Title
Health related quality of life (SF-36)
Title
Health Utility Index
Title
Respiratory function, airways hypersensitivity and inflammation and microaspiration

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male and female GERD patients aged 18-70 years with GERD symptoms. Prior long-term treatment with PPI with minimum duration of 1 year with expected future duration of at least 2 more years. Controlled on 20-40mg/day maintenance PPI therapy prior to study, defined as GERD symptom score<18 and score of 70 or more on 1-100 Global Rating Scale at screening (on medication). Increase in GERD symptom score>=15 points at baseline (off omeprazole). GERD symptom score>=18 at baseline (off omeprazole). Percent acid reflux in 24hr 4% at baseline (off omeprazole). Positive Bernstein test at baseline. Willingness to adhere to randomized treatment with availability for 3 years of follow-up. Ability to answer self and interviewer-administered questions in English. Signed informed consent. Exclusion Criteria: Aperistaltic esophagus. Severe cardiac, respiratory, hematologic or other disease constituting an unacceptable surgical risk in the investigator's opinion. Previous gastric, esophageal or anti-reflux surgery. History of malignancy within the last year with the exception of basal cell carcinoma. Pregnancy or an intention to become pregnant in the following year.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mehran Anvari, MB, BS, PhD
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
David Armstrong, MB, BCh, MA
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Charles H. Goldsmith, PhD
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Joseph's Healthcare Hamilton
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 4A6
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

A Randomized Controlled Trial of Laparoscopic Nissen Fundoplication Treatment of Patients With Chronic GERD

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