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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01055353
First Posted: January 25, 2010
Last Update Posted: May 12, 2011
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.
Information provided by:
AstraZeneca
  Purpose
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
Target Organs Damage Hypertensive no Known Cardiovascular no Known Renal Disease

Study Type: Observational
Study Design: 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

Resource links provided by NLM:


Further study details as provided by AstraZeneca:

Primary Outcome Measures:
  • 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:
  • 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
  • To describe the modalities of patient follow-up and management
  • 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.

Enrollment: 1857
Study Start Date: January 2010
Study Completion Date: June 2010
Primary Completion Date: June 2010 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
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:

  Contacts and Locations
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


  Show 908 Study Locations
Sponsors and Collaborators
AstraZeneca
Investigators
Study Director: Pascal Piedbois AstraZeneca
  More Information

Responsible Party: MC CD, AstraZeneca
ClinicalTrials.gov Identifier: NCT01055353     History of Changes
Other Study ID Numbers: NIS-CFR-DUM-2009/2
First Submitted: January 21, 2010
First Posted: January 25, 2010
Last Update Posted: May 12, 2011
Last Verified: May 2011

Keywords provided by AstraZeneca:
Target organs damage
hypertensive patients

Additional relevant MeSH terms:
Kidney Diseases
Urologic Diseases