Clinical Trials Directory

Trials / Completed

CompletedNCT00590928

Gastric pH in Critically Ill Patients

Effect of Intravenous Esomeprazole Versus Ranitidine on Gastric pH in Critically Ill Patients - a Prospective, Randomized, Double-Blind Study.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
75 (actual)
Sponsor
Medical University of Vienna · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

H2-receptor antagonists are the gold standard for stress ulcer prophylaxis in critically ill patients. Various studies demonstrated superiority of proton pump inhibitors over H2-receptor antagonists in increasing gastric pH and in healing gastric acid-dependent diseases. It is unknown, whether proton pump inhibitors are more effective in increasing gastric pH than H2-receptor antagonists in critically ill patients requiring stress ulcer prophylaxis.

Detailed description

Gastric pH is measured continuously for 72 hours with a pipolar microelectrode placed between 7 and 15cm below the lower esophageal sphincter.

Conditions

Interventions

TypeNameDescription
DRUGesomeprazole40mg once daily
DRUGranitidine50mg every h hours

Timeline

Start date
2004-07-01
Primary completion
2006-06-01
Completion
2006-06-01
First posted
2008-01-11
Last updated
2008-01-11

Locations

1 site across 1 country: Austria

Source: ClinicalTrials.gov record NCT00590928. Inclusion in this directory is not an endorsement.