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Post-marketing Clinical Study of Irbesartan <Evaluation of safety and efficacy of long-term administration>

Phase 4
Conditions
essential hypertension
Registration Number
JPRN-jRCT1080220722
Lead Sponsor
Dainippon Sumitomo Pharma Co., Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
All
Target Recruitment
100
Inclusion Criteria

Patients whose trough seated blood pressure at the end of washout period >= 160/90 mmHg or >= 150/95 mmHg

Exclusion Criteria

Patients with renal, hepatic or heart disease

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Adverse events and adverse drug reactions, etc.
Secondary Outcome Measures
NameTimeMethod
Change from baseline in trough seated diastolic blood pressure, etc.
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