drugset / Trial / NCT00573924

Trial of Oral Versus Intravenous Proton Pump Inhibitor on Intragastric pH in Patients With Bleeding Ulcers

NCT00573924

Completed 66 enrolled University of Southern California
RandomizedParallel-groupOpen-labelTreatment

Summary

Patients with bleeding ulcers identified by endoscopy will be randomly assigned to receive an acid-blocking drug (called a proton pump inhibitor \[PPI\]) either by mouth every 3 hours for 24 hours or intravenously (IV) by constant infusion for 24 hours. A pH probe in the stomach will be used to determine intragastric pH (a measure of the acid production in the stomach) at baseline and during the 24 hours of therapy. The purpose of the study is to determine if the continuous intravenous administration of the drug provides better reduction of acid in the stomach than the oral administration.

Timeline

Start
2006-02
Primary completion
Completion
2007-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Lansoprazole Other / unclassified 9 mg Oral
Comparator Lansoprazole Other / unclassified 30 mg Oral

Indications