drugset / Trial / NCT02054637

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

NCT02054637

Phase 2 Unknown 10 enrolled University Hospital Brussels
NaSingle-groupOpen-labelTreatment

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.

Timeline

Start
2014-04
Primary completion
2015-12
Completion
2016-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Lanreotide Other / unclassified 120 mg Subcutaneous

Indications