Study Completed

Arterial hypertension

Bayer Identifier:

14675

ClinicalTrials.gov Identifier:

NCT01071681

EudraCT Number:

Not Available

EU CT Number:

Not Available

Survey to assess why people are not responding to treatment in Hypertension

Trial purpose

This study will describe the factors influencing the physician in face of elevated blood pressure in already treated patients

Key Participants Requirements

Sex

Both

Age

18 - N/A

Inclusion Criteria
- Men or women over 18
- Hypertensive patients
- Uncontrolled hypertension (blood pressure >/=140/90 mmHg on the day of consultation or >/=130/80 mmHg in diabetic patients or in patients suffering from kidney failure, or in elderly patients with a systolic blood pressure >/=150 mmHg (in the absence of orthostatic hypotension)
- Patients treated with a combination, fixed or not, of Renin-Angiotensin System Blocker (RASB) + Hydrochlorothiazide (HCTZ)
- Patients examined in common medical care practice, whatever the reason for consultation
- Patients informed of the study
Exclusion Criteria

Trial summary

Enrollment Goal

1589

Trial Dates

November 2009 - February 2012

Phase

N/A

Could I Receive a placebo

Products

Kinzal/Pritor (Telmisartan, BAY68-9291)

Accepts Healthy Volunteer

Where to participate

Status	Institution	Location
Completed		Many Locations, France

Primary Outcome

Percentage of patients, according to the level of cardiovascular risk, who, at the end of the visit:- do not present any modification of hypertension treatment (therapeutic inertia) - present a change in the hypertension therapeutic
Time Frame:
on day 1
Safety Issue:
No

Secondary Outcome

Analyses of the factors that had an impact on the therapeutic decision
Time Frame:
on day 1
Safety Issue:
No

Trial design

Observational Survey Assessing the Factors of Treatment Intensification in Uncontrolled Hypertensive Patients Under a Combination Therapy, Either Fixed or not, of a Renin-Angiotensin System Blocker (RASB) and Hydrochlorothiazide (HCTZ), According to Their Level of Cardiovascular Risk.

Trial Type

Observational

Intervention Type

Drug

Trial Purpose

N/A

Allocation

N/A

Blinding

N/A

Assignment

N/A

Trial Arms

N/A

Additional Information

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