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An Epidemiological Study to Evaluate Standard Daily Practice in Managing Patients With Arterial Hypertension

Completed
Conditions
Hypertension
Registration Number
NCT01201980
Lead Sponsor
AstraZeneca
Brief Summary

This study is aimed to evaluate response rate of the antihypertensive treatment with a calcium antagonist in real life practice, to evaluate patients' quality of life and to collect the following Serbia-specific epidemiology data on hypertension: demographic data, patents characteristics, and patients' management/treatment.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
300
Inclusion Criteria
  • Subject population with essential arterial hypertension currently receiving treatment with a calcium antagonist
Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate proportion of patients on antihypertensive pharmacological treatment reaching SBP goals according to the ESC 2007 guidelines (<140 mmHg*).24 weeks
Secondary Outcome Measures
NameTimeMethod
To evaluate proportion of patients on antihypertensive pharmacological treatment reaching DBP goals according to the ESC 2007 guidelines (<90 mmHg*).24 weeks
To collect local epidemiological date on patients with hypertension (demographic data; hypertension management data: treatment, treatment changes and tolerability data).24 weeks
To evaluate patients quality of life after 12 and 24 weeks by using patients quality of life questionnaire24 weeks

Trial Locations

Locations (1)

Research Site

🇷🇸

Sremska Kamenica, Serbia

Research Site
🇷🇸Sremska Kamenica, Serbia

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