Clinical trial

Study of Esomeprazole 20 mg or 40 mg vs Placebo Effectiveness on the Occurrence…

NCT00441727 · AstraZeneca, Industry · Completed

Key facts

NCT number NCT00441727
Title Study of Esomeprazole 20 mg or 40 mg vs Placebo Effectiveness on the Occurrence of Peptic Ulcers in Subjects on Low Dose Acetylsalicylic Acid (LDA)
Official title A Randomized, Double-blind, Parallel-group, Multicentre, Phase III Study to Assess the Effect of Esomeprazole 20 or 40 mg od Versus Placebo on the Occurrence of Peptic Ulcers During 26 Weeks in Subjects on Continuous Low Dose Acetylsalicylic Acid (ASA)
Acronym Oberon
Lead sponsor AstraZeneca, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Gastric Ulcer, Duodenal Ulcer
Intervention type Drug
Interventions Esomeprazole 40 mg, Esomeprazole 20 mg, Placebo
Enrollment 2,426
Start date Feb 1, 2007
Primary completion Aug 1, 2008
Completion Aug 1, 2008
First posted Mar 1, 2007
Last update posted Jul 16, 2012
Countries Argentina, Australia, Bulgaria, Canada, Czechia, Finland, Germany, Indonesia, Mexico, Norway, Philippines, Poland and 8 more

At a glance

  • 100–999 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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