Evaluation of Atacand® (Candesartan) in Daily Medical Practice

NCT00837720 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 750

Last updated 2009-02-06

No results posted yet for this study

Summary

This open label, non-interventional study is to show the efficacy of antihypertensive treatment with Atacand in hypertensive patients. Efficacy is to be evaluated based on the difference in systolic and diastolic blood pressure at baseline and at both follow-up visits.

Conditions

Sponsors & Collaborators

Principal Investigators

  • Rok Accetto, MD · University Medical Centre Ljubljana

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-03-31
Completion
2007-06-30

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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 NCT00837720 on ClinicalTrials.gov