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NCT00767247 Clinical Trial

Analysis of Antihypertensive Treatment Efficacy

Arterial Hypertension Clinical Trial

— ATACA  

Official title:
Analysis of Antihypertensive Treatment Efficacy

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT00767247
Other study ID # NIS-CRU-ATA-2008/1
Secondary ID
Status Terminated
Phase N/A
First received October 6, 2008
Last updated December 2, 2010
Start date May 2008
Est. completion date February 2009

Study information
Verified date December 2010
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Russia: Ethics CommitteeRussia: Ministry of Health of the Russian Federation
Study type Observational

Clinical Trial Summary

Analysis of antihypertensive treatment efficacy.

Recruitment information / eligibility
Status Terminated
Enrollment 2000
Est. completion date February 2009
Est. primary completion date February 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
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

Sponsors (1)
Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Russian Federation, 

Outcome
Type Measure Description Time frame Safety issue
Primary Analysis of antihypertensive treatment efficacy. measurement BP: 3 visits for 3 month No
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