Hypertension Clinical Trial
Official title:
An Open-Label, Long-term (52-week), Safety Trial of the Fixed Dose Combination of Telmisartan 80mg Plus Hydrochlorothiazide 12.5mg and Telmisartan 40mg Plus Hydrochlorothiazide 12.5mg in Patients With Essential Hypertension - Efficacy and Safety Evaluation
The objective of this trial is to assess the safety and efficacy of 52 weeks of open-label treatment with the fixed dose combination of telmisartan 80 mg plus HCTZ 12.5 mg and telmisartan 40 mg plus HCTZ 12.5 mg in patients with essential hypertension.
This is a multi-centre study with three centres participating with a target of 30 to 90
patients entering the maintenance period and 20-60 patients completing long-term treatment
per centre. The recruitment period will be about three months from the start of the study.
Study Hypothesis:
The primary objective of this study is to demonstrate the long-term safety of a fixed dose
combination of telmisartan/HCTZ fixed-dose combination treatment. This study has no control
group; therefore, no hypothesis testing will be performed.
Comparison(s):
This study has no control group.
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