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Atacand (Candesartan) Real Life Study

A REtrospective Study on the Effects of cAndesartan vs. Losartan on Blood Pressure, Health Care Consumption and cardiovascuLar Events In a Real-liFe GP sEtting in Sweden

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00620178
Acronym
Real Life
Enrollment
14000
Registered
2008-02-21
Start date
2008-03-31
Completion date
2009-02-28
Last updated
2010-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

candesartan, losartan, blood pressure, cardiovascular disease, health care consumption

Brief summary

This study is a Swedish historical cohort study in patients prescribed Atacand or Cozaar for hypertension by selected primary care centres. Data will be extracted anonymously from electronic medical records. In addition, data regarding morbidity and mortality will be collected by merging the cohort with the following national registries: the Hospital Discharge Register (Slutenvårdsregistret), the Cause of Death Register and the Heart Intensive Care Admission (RIKS-HIA)

Interventions

DRUGCandesartan Cilexetil

oral once daily dose

DRUGLosartan

once daily oral dose

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
17 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Recorded blood pressure prior to therapy of \> 140 and/or 90 mmHg * Diagnosed as hypertensive within 15 months * First prescription of Cozaar or Atacand between 1 January 1999 and 31 December 2007, inclusive

Exclusion criteria

* Previous prescription within 15 months any drug from the ATC groups C02, C03, C07 - C09 inclusive

Design outcomes

Primary

MeasureTime frame
The primary efficacy objective is to investigate, on basis of 'first to event', the development of new cardiovascular diseases (CVD).1999 - 2007

Secondary

MeasureTime frame
Cardiovascular disease states and procedures in the background and over the entire observation period will be identified by use of ICD-9 and ICD-10 coding for diseases of the cardiovascular system. Specifically are death, acute cardiovascular events, new1999 - 2007
Health care consumption will be assessed as contacts with health care providers, in-hospital time periods for cardiovascular disease states with associated therapeutic procedures, and times spent within various levels of care (e.g. ICU and general ward).1999 - 2007

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026