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
Name Time Method 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 cilexetil 1 visit (after at least 6 months of treatment)
- Secondary Outcome Measures
Name Time Method To evaluate ventricular function after at least 6 months of treatment with candesartan cilexetil 1 visit (after at least 6 months of treatment) To gain insight into usage of candesartan cilexetil in real life for chronic heart failure in Croatia 1 visit (after at least 6 months of treatment) To evaluate patient's compliance with prescribed treatment 1 visit (after at least 6 months of treatment)
Trial Locations
- Locations (2)
Research Site
ðŸ‡ðŸ‡·Zagreb, Croatia
Reserach Site
ðŸ‡ðŸ‡·Zabok, Croatia