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CompletedNCT00709787Updated Jan 27, 2021

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

An observational study in Hypertension, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris Inc.. Completed at 2 sites in 2 countries. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2021-01-27.

Sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris Inc. · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
899
Ages
18 Years to 80 Years
Sex
All
01

Study summary

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

Read the detailed description

routine physician visits

02

Conditions studied

  • Hypertension

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Keywords

  • Epidemiology, hypertension, risk factors, coronary heart disease, patient management, compliance with medication
03

In context

Hypertension

6,689 studies on the registry are indexed under Hypertension; 965 are open to participants now.

This study's enrollment of 899 is above the median of 210 across 1,359 observational studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

Pfizer's Upjohn has merged with Mylan to form Viatris Inc. is the lead sponsor of 431 studies on the registry; none are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 8 (89%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult Hypertensive Patients managed in primary care

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

Exclusion Criteria:

  • None
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
899 participants (actual)

Groups and cohorts

  • Hypertensive Subjects undergoing primary prevention

    Other: Usual Care

Interventions

  • OtherUsual Care

    Normal care for hypertensive patients with risk factors for CHD

06

What researchers measure

Primary outcomes

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

Secondary outcomes

  1. Description of pattern of management of HT and CVD prevention, through lifestyle and use of drug therapies,

  2. Estimate adherence to treatment using the Morisky Adherence Scale (MAS)

  3. Estimation of hypertensive patients CV risk stratification based on ESH/ESC Hypertension Guidelines 2007 and to compare it with physicians' estimation of CV risk.

07

Study locations

2 sites
  • Pfizer Investigational Site
    Varazdin, 42000, Croatia
  • Pfizer Investigational Site
    Prague 4, 140 00, Czechia
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 27, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00709787
Lead sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Responsible party
Sponsor
First posted
Jul 3, 2008
Start date
Jun 2008
Primary completion
Feb 2009
Completion
Feb 2009
Last update
Jan 27, 2021

Study contacts

Pfizer CT.gov Call Center
study director · Pfizer

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2021. You cannot join it, but the record below documents what was studied.

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