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Clinical Trial Summary

REPRESS is an open label, pragmatic, multicenter, randomized controlled phase III trial with blinded endpoint with 1:1 (intervention to control arm) allocation ratio. The REPRESS trial is aimed to determine the efficacy of an educational intervention aimed at reducing dietary salt intake in elderly people (60+) with moderate hypertension and exposed to polypharmacy (3+ drugs) in improving systolic BP control compared to an attention arm.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05976477
Study type Interventional
Source Mario Negri Institute for Pharmacological Research
Contact Carlotta Franchi
Phone +39 02 39014580
Email carlotta.franchi@marionegri.it
Status Not yet recruiting
Phase N/A
Start date October 1, 2023
Completion date December 31, 2025

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