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Evaluation of Target Organs Damage in Hypertensive Patients (PreVENT-A GP)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT01055353
Recruitment Status : Completed
First Posted : January 25, 2010
Last Update Posted : May 12, 2011
Sponsor:
Information provided by:
AstraZeneca

Brief Summary:
Evaluation of target organs damage in hypertensive patients with no known cardiovascular (CV) or renal disease, stratified according to level of blood pressure control

Condition or disease
Target Organs Damage Hypertensive no Known Cardiovascular no Known Renal Disease

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Study Type : Observational
Actual Enrollment : 1857 participants
Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Evaluation of Target Organs Damage in Hypertensive Patients Followed in General Practice With no Known Cardiovascular (CV) or Renal Disease, Stratified According to Blood Pressure Control
Study Start Date : January 2010
Actual Primary Completion Date : June 2010
Actual Study Completion Date : June 2010

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Kidney Diseases




Primary Outcome Measures :
  1. To evaluate the frequency of evaluation of preclinical target organs damage in hypertensive patients with no known cardiovascular or renal disease, by taking blood pressure (controlled or uncontrolled HT*) into account [ Time Frame: once / 1 Year ]

Secondary Outcome Measures :
  1. To describe the patient profile (socio-demographic, risk factors, comorbidities, global CV risk level estimated by the doctor and calculated retrospectively [according to ESH 2007]) associated with screening for target organs damage
  2. To describe the modalities of patient follow-up and management
  3. To compare the frequency of evaluation of target organs damage as a function of the modalities of management of CV risk factors at the time of the consultation.


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
First 2 consecutive adults with hypertension, with no known cardiovascular (CV) or renal disease, seen by general practitioner
Criteria

Inclusion Criteria:

  • diagnosis of essential hypertension (treated or untreated); HT not discovered on the day of the consultation; no documented clinical cardiovascular or renal disease.

Exclusion Criteria:


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01055353


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Sponsors and Collaborators
AstraZeneca
Investigators
Layout table for investigator information
Study Director: Pascal Piedbois AstraZeneca

Layout table for additonal information
Responsible Party: MC CD, AstraZeneca
ClinicalTrials.gov Identifier: NCT01055353     History of Changes
Other Study ID Numbers: NIS-CFR-DUM-2009/2
First Posted: January 25, 2010    Key Record Dates
Last Update Posted: May 12, 2011
Last Verified: May 2011

Keywords provided by AstraZeneca:
Target organs damage
hypertensive patients

Additional relevant MeSH terms:
Layout table for MeSH terms
Kidney Diseases
Urologic Diseases