COmpliance and Efficacy in Mono and Combination Tablet Study ATacand/Atacand Plus
NCT00526279 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 9000
Last updated 2010-12-01
Summary
To evaluate compliance and patients' satisfaction in mono and combination treatment of Candesartan cilexetil (Atacand)/ Candesartan cilexetil 16mg, hydrochlorothiazide 12.5mg (Atacand plus) in hypertension.
Conditions
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Hyunah Caroline Choi · AstraZeneca Korea
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2007-06-30
- Primary Completion
- 2008-08-31
- Completion
- 2008-08-31
Countries
- South Korea
Study Locations
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