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Clinical Trials/NCT00709787
NCT00709787
Completed
Not Applicable

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

Pfizer's Upjohn has merged with Mylan to form Viatris Inc.1 site in 1 country899 target enrollmentJune 2008
ConditionsHypertension

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertension
Sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Enrollment
899
Locations
1
Primary Endpoint
Description of hypertensive patients in terms of presence of associated cardiovascular (CV) risk factors (number of additional CV risk factors and frequency)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

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

Detailed Description

routine physician visits

Registry
clinicaltrials.gov
Start Date
June 2008
End Date
February 2009
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

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

Eligibility Criteria

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

  • Not provided

Outcomes

Primary Outcomes

Description of hypertensive patients in terms of presence of associated cardiovascular (CV) risk factors (number of additional CV risk factors and frequency)

Secondary Outcomes

  • Description of pattern of management of HT and CVD prevention, through lifestyle and use of drug therapies,
  • Estimate adherence to treatment using the Morisky Adherence Scale (MAS)
  • Estimation of hypertensive patients CV risk stratification based on ESH/ESC Hypertension Guidelines 2007 and to compare it with physicians' estimation of CV risk.

Study Sites (1)

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