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Published in: Trials 1/2011

Open Access 01-12-2011 | Study protocol

Prevention of hypertension in patients with pre-hypertension: protocol for the PREVER-prevention trial

Authors: Flávio D Fuchs, Sandra C Fuchs, Leila B Moreira, Miguel Gus, Antônio C Nóbrega, Carlos E Poli-de-Figueiredo, Décio Mion, Luiz Bortoloto, Fernanda Consolim-Colombo, Fernando Nobre, Eduardo Barbosa Coelho, José F Vilela-Martin, Heitor Moreno Jr, Evandro José Cesarino, Roberto Franco, Andréa Araujo Brandão, Marcos R de Sousa, Antônio Luiz Pinho Ribeiro, Paulo Cesar Jardim, Abrahão Afiune Neto, Luiz César N Scala, Marco Mota, Hilton Chaves, João Guilherme Alves, Dario C Sobral Filho, Ricardo Pereira e Silva, José A Figueiredo Neto, Maria Cláudia Irigoyen, Iran Castro, André Avelino Steffens, Rosane Schlatter, Renato Bandeira de Mello, Francisca Mosele, Flávia Ghizzoni, Otávio Berwanger

Published in: Trials | Issue 1/2011

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Abstract

Background

Blood pressure (BP) within pre-hypertensive levels confers higher cardiovascular risk and is an intermediate stage for full hypertension, which develops in an annual rate of 7 out of 100 individuals with 40 to 50 years of age. Non-drug interventions to prevent hypertension have had low effectiveness. In individuals with previous cardiovascular disease or diabetes, the use of BP-lowering agents reduces the incidence of major cardiovascular events. In the absence of higher baseline risk, the use of BP agents reduces the incidence of hypertension. The PREVER-prevention trial aims to investigate the efficacy, safety and feasibility of a population-based intervention to prevent the incidence of hypertension and the development of target-organ damage.

Methods

This is a randomized, double-blind, placebo-controlled clinical trial, with participants aged 30 to 70 years, with pre-hypertension. The trial arms will be chlorthalidone 12.5 mg plus amiloride 2.5 mg or identical placebo. The primary outcomes will be the incidence of hypertension, adverse events and development or worsening of microalbuminuria and of left ventricular hypertrophy in the EKG. The secondary outcomes will be fatal or non-fatal cardiovascular events: myocardial infarction, stroke, heart failure, evidence of new sub-clinical atherosclerosis, and sudden death. The study will last 18 months. The sample size was calculated on the basis of an incidence of hypertension of 14% in the control group, a size effect of 40%, power of 85% and P alpha of 5%, resulting in 625 participants per group. The project was approved by the Ethics committee of each participating institution.

Discussion

The early use of blood pressure-lowering drugs, particularly diuretics, which act on the main mechanism of blood pressure rising with age, may prevent cardiovascular events and the incidence of hypertension in individuals with hypertension. If this intervention shows to be effective and safe in a population-based perspective, it could be the basis for an innovative public health program to prevent hypertension in Brazil.

Trial Registration

Clinical Trials NCT00970931.
Appendix
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Metadata
Title
Prevention of hypertension in patients with pre-hypertension: protocol for the PREVER-prevention trial
Authors
Flávio D Fuchs
Sandra C Fuchs
Leila B Moreira
Miguel Gus
Antônio C Nóbrega
Carlos E Poli-de-Figueiredo
Décio Mion
Luiz Bortoloto
Fernanda Consolim-Colombo
Fernando Nobre
Eduardo Barbosa Coelho
José F Vilela-Martin
Heitor Moreno Jr
Evandro José Cesarino
Roberto Franco
Andréa Araujo Brandão
Marcos R de Sousa
Antônio Luiz Pinho Ribeiro
Paulo Cesar Jardim
Abrahão Afiune Neto
Luiz César N Scala
Marco Mota
Hilton Chaves
João Guilherme Alves
Dario C Sobral Filho
Ricardo Pereira e Silva
José A Figueiredo Neto
Maria Cláudia Irigoyen
Iran Castro
André Avelino Steffens
Rosane Schlatter
Renato Bandeira de Mello
Francisca Mosele
Flávia Ghizzoni
Otávio Berwanger
Publication date
01-12-2011
Publisher
BioMed Central
Published in
Trials / Issue 1/2011
Electronic ISSN: 1745-6215
DOI
https://doi.org/10.1186/1745-6215-12-65

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