Hypertension Clinical Trial
Official title:
Efficacy and Safety of the Fixed-dose Combination of Valsartan Plus Chlorthalidone Vs Valsartan or Chlorthalidone Alone in the Treatment of Arterial Hypertension, Open-label, Controlled, Randomized and Multicenter Trial
This trial is aimed to assess the efficacy and safety of a fixed-dose combination therapy with Valsartan and Chlorthalidone, Vs Valsartan or Chlorthalidone alone for treatment of adult patients with diagnosis of arterial hypertension.
In spite of the existence of a great variety of treatments with drugs effective against
arterial hypertension, the percentages of arterial hypertension control with monotherapy
remain quite low reason why the fixed-dose combinations of drugs have been one of the most
interesting research topics in order to achieve an appropriate control of arterial
hypertension.
The possibility of achieving better coverage and Blood Pressure control through a drug
combination has leaded, on a scientific base of the efficacy of an Angiotensin Receptor
Blockers II plus diuretic combination, to the development of a great number of combinations
with different Angiotensin II Receptor Blockers plus hydrochlorothiazide. Yet it is
noteworthy that despite the increasing evidence showing additional benefits in Blood
pressure control and reduction of cardiovascular outcomes with chlorthalidone over
hydrochlorothiazide, there is neither a great number of combinations nor studies with
Angiotensin II Receptor Blockers plus chlorthalidone whereby the conduction of a trial
assessing the efficacy and safety of Valsartan plus chlorthalidone in hypertensive patients
is proposed plus the benefits of combination therapy that include, among others, the greater
efficacy with lower doses of each individual component as well as reduction in occurrence of
adverse events directly related with lower drug doses.With this treatment schedule it is
expected to obtain higher control of blood pressure values and greater percentage of
patients.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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