Overview
Compare Efficacy of Gastric Acid Suppression by Oral and Intravenous Administration of Esomeprazole in Patients With Peptic Ulcer
Status:
Unknown status
Unknown status
Trial end date:
2007-09-01
2007-09-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to compare the gastric acid suppression profile among different regimen (Oral Vs Intravenous)of administration of proton pump inhibitor - Esomeprazole by 24hours intragastric pH monitoring.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Pamela Youde Nethersole Eastern HospitalTreatments:
Esomeprazole
Criteria
Inclusion Criteria:1. Patients with non-bleeding peptic ulcer which do not require endoscopic therapy.
2. Chinese, Age ³18 and <90
3. Provision of an informed written consent signed by the patient.
Exclusion Criteria:
1. Treatment of antisecretory drugs during the preceding 4 weeks
2. The present inter-current ulcer complication (gastric outlet obstruction or ulcer
perforation)
3. Presence of esophageal / gastric varices
4. aspirin or NSAID user
5. Pregnancy
6. Age <18 or >90
7. Moribund patients, patients with severe liver or renal disease
8. Known sensitivity to proton pump inhibitors
9. Previous gastric surgery (except simple patch repair)
10. Patient unable to give written consent
11. Special population, e.g. prisoner, mentally disabled, investigators' student or
employees