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Candesartan and Candesartan/ Hydrochlorothiazide in the Treatment of Patients With Hypertension and LVH — CandLE  

Essential Hypertension Clinical Trial

Official title:
Candesartan and Candesartan/ Hydrochlorothiazide in the Treatment of Patients With Essential Hypertension and a Concomitant Disease Left Ventricular Hypertrophy

Clinical Trial Summary

The CandLE study with at maximum daily dose of 32 mg candesartan or 16/12.5 mg candesartan/hydrochlorothiazide has the objective to evaluate under naturalistic conditions, i.e. under routine medical care conditions, the impact of the antihypertensive therapy with candesartan or candesartan/HCT on relevant medical parameters related to the left ventricular hypertrophy (LVH) as well as the efficacy and tolerability of candesartan or candesartan/HCT in subjects suffering from essential hypertension..

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00607633
Study type Observational
Source AstraZeneca
Contact
Status Completed
Phase N/A
Start date January 2007
Completion date October 2007
View Details
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