Clinical Trial: Resolving Bile Reflux by Lanreotide in Patients With Roux-en-Y Gastrojejunostomy

Study Status: Not yet recruiting
Recruit Status: Unknown status
Study Type: Interventional




Official Title: Resolving Bile Reflux by Lanreotide in Patients With Roux-en-Y Gastrojejunostomy

Brief Summary:

Somatostatine induces a dose-dependent reduction of postprandial plasma cholecystokinin (CCK) secretion with a concomitant inhibition of postprandial gallbladder contraction, abolishing almost completely bile salts output from the gallbladder. Somatostatine is also known to decrease acid production with significant increase of intragastric pH. In this way, somatostatine could influence acid as well as non-acid reflux by decreasing gallbladder emptying and decreasing acid secretion.

Purpose of the study is to evaluate the efficacy of lanreotide autogel 120 mg on symptoms and endoscopic lesions in patients with an endoscopic gastrointestinal reflux esophagitis that cannot be controlled with classic therapy.