Clinical trial for the practical use of a metalic connector for assisted circulation system
Not Applicable
- Conditions
- Severe heart failure
- Registration Number
- JPRN-UMIN000022339
- Lead Sponsor
- Tohoku University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Not provided
Exclusion Criteria
Exclusion criteria are as folows. patients with irrecoverable renal failure patients with irrecoverable liver failure patients with respiratory failure without heart failure patinets with severe bleeding tedency small sized child patients patients with allergy to metal
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The frequency of exchange of support device accompanied with thrombosis in the connector. The incidence of thromboembolic events
- Secondary Outcome Measures
Name Time Method 30-day mortality frequency of adverse event (hemorrhagic complications) renal function (Creatinine) liver functin (AST, ALT and LDH)