Achievement of Goal Resting Heart Rate on B-blockers in Patients With Stable Angina and Hypertension

NCT ID: NCT01321242

Last Updated: 2012-06-01

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

400 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-04-30

Study Completion Date

2011-08-31

Brief Summary

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This is a multicenter survey of Russian data on target heart rate achievement in patients with stable angina and arterial hypertension who are currently treated with beta-blockers for at least 2 months and with no dose change for a minimum of 4 weeks

Detailed Description

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Conditions

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Stable Angina Hypertension

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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achieving resting HR goals

Patient population will be comprised of typical for cardiological practice sample of patients with Coronary Heart Disease and arterial hypertension administered beta-blockers, subjects achieving resting HR goals, according to ACC/AHA/ACP-ASIM Guidelines

No interventions assigned to this group

non-achieving HR goals

Patient population will be comprised of typical for cardiological practice sample of patients with Coronary Heart Disease and arterial hypertension administered beta-blockers, subjects non-achieving HR goals, according to ACC/AHA/ACP-ASIM Guidelines

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Stable angina I-III class by the Canadian Cardiovascular Society Classification and concomitant primary hypertension
* Subject is on beta-blockers treatment for at least 2 months prior to inclusion into survey, with no dose change for a minimum of 4 weeks

Exclusion Criteria

* Use of phenylalkylamine and benzothiazepine calcium channel blockers
* Hemodynamic significant mitral and aortic valve disease
* Acute myocardial infarction and unstable angina within 3 months before enrolment
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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AstraZeneca

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Alexey Stepanov

Role: STUDY_DIRECTOR

AstraZeneca

Z.D. Kobalava

Role: PRINCIPAL_INVESTIGATOR

The Russian Peoples' Friendship University, Municipal Clinical Hospital #64

Locations

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Research Site

Moscow, , Russia

Site Status

Research Site

Rostov-on-Don, , Russia

Site Status

Research Site

Saint Petersburg, , Russia

Site Status

Research Site

Saratov, , Russia

Site Status

Research Site

Ulyanovsk, , Russia

Site Status

Research Site

Yekaterinburg, , Russia

Site Status

Countries

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Russia

References

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Kobalava Z, Khomitskaya Y, Kiyakbaev G; ATHENA trial investigators. AchievemenT of target resting HEart rate on beta-blockers in patients with stable angiNA and hypertension (ATHENA) in routine clinical practice in Russia. Curr Med Res Opin. 2014 May;30(5):805-11. doi: 10.1185/03007995.2013.874993. Epub 2014 Jan 17.

Reference Type DERIVED
PMID: 24400847 (View on PubMed)

Other Identifiers

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NIS-CRU-ATC-2011/1

Identifier Type: -

Identifier Source: org_study_id

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