drugset / Trial / NCT00441727

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)

NCT00441727 ↗

Phase 3 Completed 2426 enrolled AstraZeneca
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to compare the effect of esomeprazole 20 or 40 mg once daily versus placebo on the occurrence of peptic ulcers during 26 weeks in subjects on continuous low-dose acetylsalicylic acid.

Timeline

Start
2007-02
Primary completion
2008-08
Completion
2008-08

Outcome

Met primary endpoint

paper 1.5% of esomeprazole 40 mg and 1.1% of esomeprazole 20 mg recipients, compared with 7.4% of placebo recipients, developed peptic ulcers (both p<0.0001 vs placebo). PMID 21415072 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Esomeprazole Small molecule 20 mg —
Subject Esomeprazole Small molecule 40 mg —