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Assessment of the effects on 24-hour ambulatory blood pressure and the safety of a once-a-day oral 8 mg perindopril morning administration versus evening administration in hypertensive patients. An 8-week, 2-arm, randomised, double-blind study.

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Study Phase

Phase 2

Therapeutic Area

Cardiovascular Diseases

SponsorInstitut de Recherches Internationales Servier (I.R.I.S)
Active substance/
Medical device


Active Substance CodeS009490
Protocol CodeCL2-09490-157
EudraCT Code2007-007026-22

Documents and links

Results summary READ MORE

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