A Randomized Controlled Trial of Laparoscopic Nissen Fundoplication Treatment of Patients With Chronic GERD
Information source: Hamilton Health Sciences
Information obtained from ClinicalTrials.gov on December 31, 2007 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Gastroesophageal Reflux
Intervention: Proton Pump Inhibitors (Drug); Laparoscopic Nissen Fundoplication (Procedure)
Phase: N/A
Status: Active, not recruiting
Sponsored by: Hamilton Health Sciences Official(s) and/or principal investigator(s): Mehran Anvari, MB, BS, PhD, Principal Investigator, Affiliation: McMaster University, Hamilton, Ontario, Canada David Armstrong, MB, BCh, MA, Principal Investigator, Affiliation: McMaster University, Hamilton, Ontario, Canada Charles H. Goldsmith, PhD, Principal Investigator, Affiliation: McMaster University, Hamilton, Ontario, Canada
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.
Clinical Details
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 design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
Primary outcome: GERD Symptom ScaleSymptom-free Day Measurement Cost Measurement
Secondary outcome: 24-hour pHEconomic Analysis Endoscopy Esophageal manometry Health related quality of life (SF-36) Health Utility Index Respiratory function, airways hypersensitivity and inflammation and microaspiration
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 PPE's have
proven more efficacious than H2RAs.
Eligibility
Minimum age: 18 Years.
Maximum age: 70 Years.
Gender(s): Both.
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.
Locations and Contacts
St. Joseph's Healthcare Hamilton, Hamilton, Ontario L8N 4A6, Canada
Additional Information
Starting date: January 2000
Ending date: September 2007
Last updated: June 22, 2006
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