Efficacy Observational Study of Candesartan Cilexetil on Hypertensive Patients
NCT00573742 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1940
Last updated 2010-08-19
Summary
The purpose of this study is to observe treatment with candesartan cilexetil 16mg for 8 weeks, in uncontrolled hypertensive patients, in improvement of achieving of treatment goals and impact on blood pressure level in patients with uncontrolled hypertension treated with candesartan cilexetil.
Conditions
- Primary Hypertension
Interventions
- DRUG
-
Candesartan Cilexeotil 16mg
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Mihai Isvoranu · AstraZeneca
-
Gabriela Teodorescu · AstraZeneca
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2007-09-30
- Primary Completion
- 2008-02-29
- Completion
- 2008-02-29
Countries
- Romania
Study Locations
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