A Randomized Controlled Trial of Laparoscopic Nissen Fundoplication Treatment of Patients With Chronic GERD
Gastroesophageal Reflux
About this trial
This is an interventional treatment trial for Gastroesophageal Reflux
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.
Sites / Locations
- St. Joseph's Healthcare Hamilton
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Proton Pump Inhibitor
Laparoscopic Nissen Fundoplication
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.