In-practice Evaluation of Atacand 16mg Antihypertensive Effect

NCT00802542 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 400

Last updated 2010-12-03

No results posted yet for this study

Summary

The purpose of this study is to prove in practice the effectiveness of Atacand 16 mg in reducing blood pressure after 4 weeks of administration and the importance of administration of adequate doses

Conditions

  • Essential Hypertension

Sponsors & Collaborators

Principal Investigators

  • Agrita Hartmane · AstraZeneca

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-11-30
Primary Completion
2009-01-31
Completion
2009-01-31

Countries

  • Latvia

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 NCT00802542 on ClinicalTrials.gov