A clinical study for FS-311(hemodiafilter)
Not Applicable
- Conditions
- Renal failure
- Registration Number
- JPRN-UMIN000018858
- 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 who are pregnant or suspected to be pregnant, patients who are breast-feeding 2)Patients who are judged to be unable to attend this study as cardiovascular diseases by the investigator 3)Patients who have severe anemias or severe cardiovascular complications, patients who have severe arteriosclerosis obliterans 4)Patients with a history of allergy against extracorporeal circulation therapy 5)Other patients who are considerd ineligible for this study by the investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1)adverse events 2)Device deficiencies 3)blood compatibility(change of a white blood-cell count and platelets count during the HDF session)
- Secondary Outcome Measures
Name Time Method