The Cardiac Insufficiency BIsoprolol Study in Japanese Patients with Chronic Heart Failure
- Conditions
- Chronic heart failure
- Registration Number
- JPRN-UMIN000011274
- Lead Sponsor
- CIBIS-J study group
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 220
Not provided
Patients who meet any of the following exclusion criteria at the time of registration will be excluded: (1) Patients who are considered not to be candidates for administration of bisoprolol or carvedilol. (2) Patients who have developed acute myocardial infarction within 8 weeks before the registration day. (3) Patients who have history of stroke or serious cerebrovascular accident within 1 year before the registration day. (4) Patients with poor prognosis and life-threatening disease, such as malignant tumor, or such medical history within 5 years before the registration day. (5) Patients who are scheduled to undergo coronary revascularization (CABG, PCI) during the study period. (6) Patients who are pregnant, lactating, may become pregnant, or want to become pregnant during the study. (7) Patients from whom written informed consent cannot be obtained. (8) Patients who are judged by an investigator to be inappropriate for this study for any other reason.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method