Efficacy Observational Study of Candesartan Cilexetil on Hypertensive Patients

NCT00573742 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1940

Last updated 2010-08-19

No results posted yet for this study

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

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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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 NCT00573742 on ClinicalTrials.gov