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A Study to Prevent Rebleeding After Initial Successful Primary Endoscopic Haemostasis of a Bleeding Peptic Ulcer

AstraZeneca logo

AstraZeneca

Status and phase

Completed
Phase 3

Conditions

Gastrointestinal Hemorrhage

Treatments

Drug: Esomeprazole

Study type

Interventional

Funder types

Industry

Identifiers

NCT00251979
D961DC00001

Details and patient eligibility

About

This study is being carried out to see if constant 3 days infusion of Nexium is effective in preventing rebleeding after an endoscopic treatment.

Enrollment

1,312 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Signs of a bleeding in the stomach
  • One endoscopically confirmed bleeding ulcer in the stomach or duodenum

Exclusion criteria

  • Malignancy or other advanced disease.
  • Major cardiovascular event.
  • Severe hepatic disease

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

79

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Data sourced from clinicaltrials.gov

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