COmpliance and Efficacy in Mono and Combination Tablet Study ATacand/Atacand Plus

NCT00526279 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 9000

Last updated 2010-12-01

No results posted yet for this study

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

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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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00526279 on ClinicalTrials.gov