Analysis of Antihypertensive Treatment Efficacy (ATACA)

This study has been terminated.
Sponsor:
Information provided by:
AstraZeneca
ClinicalTrials.gov Identifier:
NCT00767247
First received: October 6, 2008
Last updated: December 2, 2010
Last verified: December 2010
  Purpose

Analysis of antihypertensive treatment efficacy.


Condition
Arterial Hypertension

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Official Title: Analysis of Antihypertensive Treatment Efficacy

Resource links provided by NLM:


Further study details as provided by AstraZeneca:

Primary Outcome Measures:
  • Analysis of antihypertensive treatment efficacy. [ Time Frame: measurement BP: 3 visits for 3 month ] [ Designated as safety issue: No ]

Estimated Enrollment: 2000
Study Start Date: May 2008
Study Completion Date: February 2009
Primary Completion Date: February 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts
1
Male or female with arterial hypertension

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

outpatient clinics

Criteria

Inclusion Criteria:

  • arterial hypertension
  • intake of Atacand before study enrollment

Exclusion Criteria:

  • hypersensitivity to candesartan or any other ingredient of Atacand
  • liver function impairment and/or cholestasis
  • severe renal insufficiency (serum creatinine > 265 µmol/L)
  • Pregnant and lactating women
  Contacts and Locations
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00767247

Locations
Russian Federation
Research Site
Arhangelsk, Russian Federation
Research Site
Bryansk, Russian Federation
Research Site
Domodedovo, Russian Federation
Research Site
Dzerzhinsk, Russian Federation
Research Site
Ekaterinburg, Russian Federation
Research Site
Essentuki, Russian Federation
Research Site
Georgievsk, Russian Federation
Research Site
Irkutsk, Russian Federation
Research Site
Kazan, Russian Federation
Research Site
Samara, Russian Federation
Research Site
Severodvinsk, Russian Federation
Research Site
Vidnoe, Russian Federation
Research Site
Volgograd, Russian Federation
Sponsors and Collaborators
AstraZeneca
Investigators
Principal Investigator: Dmitry Zateyshchikov, MD, Prof Federal State Institution of Russian President's General Management Department
  More Information

No publications provided

Responsible Party: Andrey Strugovshchikov, Medical Director, Astra Zeneca, Russia
ClinicalTrials.gov Identifier: NCT00767247     History of Changes
Other Study ID Numbers: NIS-CRU-ATA-2008/1
Study First Received: October 6, 2008
Last Updated: December 2, 2010
Health Authority: Russia: Ethics Committee
Russia: Ministry of Health of the Russian Federation

Keywords provided by AstraZeneca:
Arterial Hypertension

Additional relevant MeSH terms:
Hypertension
Vascular Diseases
Cardiovascular Diseases
Antihypertensive Agents
Cardiovascular Agents
Therapeutic Uses
Pharmacologic Actions

ClinicalTrials.gov processed this record on August 18, 2014