Working…
COVID-19 is an emerging, rapidly evolving situation.
Get the latest public health information from CDC: https://www.coronavirus.gov.

Get the latest research information from NIH: https://www.nih.gov/coronavirus.
ClinicalTrials.gov
ClinicalTrials.gov Menu

RIAT Registry: Reason for Not Intensifying Antihypertensive Treatment (RIAT)

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: NCT00258921
Recruitment Status : Completed
First Posted : November 28, 2005
Last Update Posted : November 22, 2007
Sponsor:
Collaborator:
Bristol-Myers Squibb
Information provided by:
Sanofi

Brief Summary:
To support physicians in their active management of hypertensive patients. By targeting specific systolic and diastolic blood pressure (BP) figures physicians will closely monitor the BP values and as such will have an individualized control of the treatment in each patient.

Condition or disease
Hypertension

Layout table for study information
Study Type : Observational
Enrollment : 31870 participants
Time Perspective: Prospective
Official Title: An International Registry in Essential Hypertension
Study Start Date : March 2004
Actual Study Completion Date : July 2006

Resource links provided by the National Library of Medicine






Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

The following information on clinical trials is provided for information purposes only to allow patients and physicians to have an initial discussion about the trial. This information is not intended to be complete information about the trial, to contain all considerations that may be relevant to potential participation in the trial, or to replace the advice of a personal physician or health professional.

Main criteria are listed hereafter:

Inclusion Criteria:

  • Adult hypertensive
  • Either newly diagnosed and untreated
  • or previously treated and uncontrolled Patients of both sexes with essential hypertension

Exclusion Criteria:

  • Known secondary hypertension
  • Known secondary curable hypertension (i.e. pheochromocytoma, aldosterone producing adenoma, Cushing disease). Patients with renal disease are not excluded.

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): NCT00258921


Sponsors and Collaborators
Sanofi
Bristol-Myers Squibb
Investigators
Layout table for investigator information
Study Director: Pascale BLONDIN, MD Sanofi

Layout table for additonal information
ClinicalTrials.gov Identifier: NCT00258921    
Other Study ID Numbers: R-9511
First Posted: November 28, 2005    Key Record Dates
Last Update Posted: November 22, 2007
Last Verified: November 2007
Additional relevant MeSH terms:
Layout table for MeSH terms
Hypertension
Vascular Diseases
Cardiovascular Diseases