Clinical trial

A Study to Prevent Rebleeding After Initial Successful Primary Endoscopic…

NCT00251979 · AstraZeneca, Industry · Completed

Key facts

NCT number NCT00251979
Title A Study to Prevent Rebleeding After Initial Successful Primary Endoscopic Haemostasis of a Bleeding Peptic Ulcer
Official title A Randomised, Double-blind, Parallel-group, Placebo Controlled Study of Esomeprazole i.v. (Bolus Infusion of 80 mg Followed by a Continuous Infusion of 8 mg Per Hour) Administered for 72 Hours to Assess Prevention of Rebleeding in Subjects That Have Undergone Successful Primary Endoscopic…
Lead sponsor AstraZeneca, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Gastrointestinal Hemorrhage
Intervention type Drug
Interventions Esomeprazole
Enrollment 1,312
Start date Oct 1, 2005
Primary completion Dec 1, 2007
Completion Dec 1, 2007
First posted Nov 11, 2005
Last update posted Jun 17, 2011
Countries Austria, Denmark, Finland, France, Germany, Greece, Hong Kong, Netherlands, Norway, Romania, Russia, South Africa and 4 more

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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