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Evaluation of Clinical Signs and Symptoms of Chronic Heart Failure in Patients Treated With Candesartan Cilexetil in Croatia

Completed
Conditions
Chronic Heart Failure
Registration Number
NCT00984529
Lead Sponsor
AstraZeneca
Brief Summary

The purpose of this study is to determine whether treatment with candesartan cilexetil for at least 6 months in patients with chronic heart failure improves clinical signs and symptoms of chronic heart failure.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
500
Inclusion Criteria
  • Patients with diagnosed chronic heart failure
  • Patients treated for at least 6 months with candesartan cilexetil
  • Signed Informed consent
Exclusion Criteria
  • Hypersensitivity to candesartan cilexetil
  • Pregnancy / lactation
  • Severe hepatic impairment

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate clinical signs and symptoms of chronic heart failure (in terms of NYHA status, fluid retention and tiredness/fatigue) after at least 6 months of treatment with candesartan cilexetil1 visit (after at least 6 months of treatment)
Secondary Outcome Measures
NameTimeMethod
To evaluate ventricular function after at least 6 months of treatment with candesartan cilexetil1 visit (after at least 6 months of treatment)
To gain insight into usage of candesartan cilexetil in real life for chronic heart failure in Croatia1 visit (after at least 6 months of treatment)
To evaluate patient's compliance with prescribed treatment1 visit (after at least 6 months of treatment)

Trial Locations

Locations (2)

Research Site

🇭🇷

Zagreb, Croatia

Reserach Site

🇭🇷

Zabok, Croatia

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