Epidemiological Study In Hypertensive Patients: Assessment Of Risk Factors Prevalence And Of Patients' Management

NCT ID: NCT00709787

Last Updated: 2021-01-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

899 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-06-30

Study Completion Date

2009-02-28

Brief Summary

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To assess the pattern of hypertension in the population in terms of presence of additional risk factors (ARF) and cardiovascular risk stratification.

Detailed Description

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routine physician visits

Conditions

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Hypertension

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Hypertensive Subjects undergoing primary prevention

Usual Care

Intervention Type OTHER

Normal care for hypertensive patients with risk factors for CHD

Interventions

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Usual Care

Normal care for hypertensive patients with risk factors for CHD

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age 18 to 80 years old
* Patients with hypertension: newly diagnosed and /or already diagnosed and treated , whether at goal or not for the blood pressure level;
* Patients with no history of CHD/CVD

Exclusion Criteria

* None
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer's Upjohn has merged with Mylan to form Viatris Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

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Pfizer Investigational Site

Varaždin, , Croatia

Site Status

Pfizer Investigational Site

Prague, , Czechia

Site Status

Countries

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Croatia Czechia

Other Identifiers

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A3841059

Identifier Type: -

Identifier Source: org_study_id

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