Clinical Trials Directory

Trials / Completed

CompletedNCT00625274

A Randomized, Open-Label, Comparative 3-Way Treatment Crossover Study of 24-Hour Intragastric pH Profile of Once Daily Oral Administration of Esomeprazole 40mg, Lansoprazole 30mg, and Pantoprazole 40mg at Steady State in NSAID-Using Patients

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
AstraZeneca · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

This study looks at controlling intragastric pH following administration of esomeprazole 40 mg, lansoprazole 30 mg and pantoprazole 40 mg taken orally, once daily in patients taking either non-selective or cyclooxygenase-2 (COX-2) selective nonsteroidal anti-inflammatory drugs (NSAIDs).

Conditions

Interventions

TypeNameDescription
DRUGEsomeprazole40mg Oral
DRUGLansoprazole30mg Oral
DRUGPantoprazole40mg Oral

Timeline

Start date
2004-06-01
Primary completion
2004-11-01
Completion
2004-11-01
First posted
2008-02-28
Last updated
2008-02-28

Source: ClinicalTrials.gov record NCT00625274. Inclusion in this directory is not an endorsement.