Overview

An Open Label pH Comparison of Esomeprazole and Lansoprazole in Barrett's Esophagus Patients

Status:
Completed
Trial end date:
2007-04-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of the study is to compare the treatment of esomeprazole 40 mg once daily and lansoprazole 30 mg once daily in controlling intragastric pH in Barrett's Esophagus patients
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
AstraZeneca
Treatments:
Dexlansoprazole
Esomeprazole
Lansoprazole
Criteria
Inclusion Criteria:

- Documented history (within 2 yrs of histologically proven BE;

- Aged 18-70 (inclusive);

- Willing and able to comply with all study procedures

Exclusion Criteria:

- Signs of clinically significant GI bleeding within 3 days prior to randomization;

- History of gastric or esophageal surgery;

- Clinically significant illness within 2 weeks prior to first dose of study drug or
during study