Clinical Trials Directory

Trials / Completed

CompletedNCT01136317

Comparison of Antisecretory Effect of a Single Dose of Rabeprazole 20 mg and Omeprazole 20 mg in Obese Subjects

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
Sponsor
Nantes University Hospital · Academic / Other
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

This study aims to determine, in obese subjects, the antisecretory effect of a single dose of placebo, rabeprazole 20 mg and omeprazole 20 mg using 24h gastric pH monitoring, in a prospective, monocentre, randomized manner. Monitorings are separated between 6 and10 days. The main outcome criteria of analysis is the percentage of time with gastric pH above 3 during 24hours.

Conditions

Interventions

TypeNameDescription
DRUGOmeprazole
DRUGRabeprazole
DRUGLactose

Timeline

Start date
2010-04-01
Primary completion
2010-07-01
Completion
2010-07-01
First posted
2010-06-03
Last updated
2010-09-24

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT01136317. Inclusion in this directory is not an endorsement.