RIAT Registry: Reason for Not Intensifying Antihypertensive Treatment

NCT ID: NCT00258921

Last Updated: 2007-11-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

31870 participants

Study Classification

OBSERVATIONAL

Study Start Date

2004-03-31

Study Completion Date

2006-07-31

Brief Summary

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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.

Detailed Description

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Conditions

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Hypertension

Study Design

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Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bristol-Myers Squibb

INDUSTRY

Sponsor Role collaborator

Sanofi

INDUSTRY

Sponsor Role lead

Principal Investigators

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Pascale BLONDIN, MD

Role: STUDY_DIRECTOR

Sanofi

Other Identifiers

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R-9511

Identifier Type: -

Identifier Source: org_study_id