Morbid Obesity Clinical Trial
Official title:
Randomized, Prospective, Double-blind Trial of PPI vs Placebo in Prevention of Gastrojejunal Strictures After Laparoscopic Roux-en-Y Gastric Bypass for Morbid Obesity
The purpose of this study is to determine whether suppressing acid production by administration of daily proton pump inhibitors in the early post-operative period will reduce the gastrojejunal anastomosis stricture rate in patients undergoing laparoscopic gastric bypass surgery for morbid obesity.
Laparoscopic Roux-en-Y gastric bypass (LYRGB) has been shown to be a safe and effective
procedure for the treatment of morbid obesity. However, a common early complication of LYRGB
is stricture at the gastrojejunal (GJ) anastomosis, occurring in 4% - 27% of patients,
usually within the third post-operative month. This complication usually presents with
progressive dysphagia leading to daily vomiting. Endoscopic balloon dilation is the
treatment of choice for this complication, and multiple dilations are often required to
provide complete resolution.
The etiology of GJ anastomotic strictures is unknown and is probably multi-factorial. Some
investigators hypothesize that ischemia or non-ischemia-related excessive scar formation is
the cause of stricture. The method of construction of the anastomosis as well seems to have
an impact, as circular stapled anastomoses may have higher rates of stricture than linear
staplers or completely hand-sewn anastomoses. The route of the Roux limb (antecolic vs
retrocolic) does not appear to affect this complication.
Several investigators have demonstrated little acid production in the gastric bypass pouch.
Despite this data, acid secretion has been hypothesized as a predominant factor in the
development of GJ stricture. This hypothesis is supported in part by the frequent finding of
ulcers at the site of stricture in up to 55% of patients. The purpose of this study is to
determine whether suppressing acid production by administration of daily proton pump
inhibitors in the early post-operative period will reduce GJ anastomosis stricture rate.
PLEASE NOTE: THIS STUDY DOES NOT PROVIDE SURGERY (APPROPRIATE INSURANCE COVERAGE IS
REQUIRED).
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention
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