A clinical study for TBP-101 (CHDF hemofilter)
Not Applicable
- Conditions
- Acute Kidney Injury
- Registration Number
- JPRN-UMIN000028674
- Lead Sponsor
- Toray Industries,Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 14
Inclusion Criteria
Not provided
Exclusion Criteria
1)Patients with disease hard to be treated by CRRT, such as Heparin-Induced Thrombocytopenia (HIT). 2)Patients with anamnesis of allergy symptoms such as anaphylaxis caused by dialyzer, hemofilter et al.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1)Average hours the investigational device is used 2)Adverse events 3)Device deficiencies
- Secondary Outcome Measures
Name Time Method