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Clinical Trial Summary

This is a multicenter, randomized, double-blind, parallel-group, dose-ranging, comparator-controlled study of the effect of pantoprazole on intragastric pH after successful endoscopic hemostasis in hospitalized patients. Patients will receive either intravenous pantoprazole (one of two regimens) or ranitidine (the comparator) within 2 hours of successful hemostasis and administration will continue for 72 hours after hemostasis.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT00037570
Study type Interventional
Source Wyeth is now a wholly owned subsidiary of Pfizer
Contact
Status Completed
Phase Phase 2
Start date November 2000
Completion date February 2002

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