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
| Type | Name | Description |
|---|---|---|
| DRUG | Esomeprazole | 40mg Oral |
| DRUG | Lansoprazole | 30mg Oral |
| DRUG | Pantoprazole | 40mg 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.