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Study Evaluating Pantoprazole in Peptic Ulcer Hemorrhage

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Wyeth

Status and phase

Completed
Phase 3

Conditions

Peptic Ulcer Hemorrhage

Treatments

Drug: Pantoprazole

Study type

Interventional

Funder types

Industry

Identifiers

NCT00040495
3001K2-315

Details and patient eligibility

About

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.

Enrollment

149 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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