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Study Evaluating Pantoprazole in Peptic Ulcer Hemorrhage

An Efficacy and Safety Study of Intravenous Pantoprazole in the Prevention of Recurrent Peptic Ulcer Bleeding After Successful Hemostasis

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00040495
Enrollment
149
Registered
2002-06-28
Start date
2001-04-30
Completion date
2003-01-31
Last updated
2013-02-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Peptic Ulcer Hemorrhage

Keywords

Peptic, Ulcer, Hemorrhage

Brief summary

The purpose of this study is to evaluate the efficacy and safety of intravenous pantoprazole in the prevention of rebleeding in patients with bleeding peptic ulcer disease after successful endoscopic hemostatic therapy.

Interventions

DRUGPantoprazole

Sponsors

Wyeth is now a wholly owned subsidiary of Pfizer
Lead SponsorINDUSTRY

Study design

Primary purpose
PREVENTION

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients must be men or non-pregnant women at least 18 years of age * Patients who present with a gastric or duodenal ulcer

Exclusion criteria

* Patients with ulcer appearance of clean base (non-oozing, non-spurting) or flat pigmented spot; adherent clots not removed by irrigation * Patients presenting with active bleeding and/or NBVV at 2 or more separate sites * Patients with any severe concomitant diseases, eg, end stage liver or renal disease, or unstable cardiovascular, pulmonary, renal, hepatic, or gastrointestinal diseases

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026