A clinical study for FS-501 (hollow fiber dialyzer)
Not Applicable
- Conditions
- Renal failure
- Registration Number
- JPRN-UMIN000019853
- Lead Sponsor
- Toray Industries, Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 28
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patient who is pregnant, suspected to be pregnant, or lactating. 2) Patient who has been judged to be unable to participate in this study by the investigator for unstable heart or hemodynamics. 3) Patient who has a severe anemias, severe cardiovascular complications, or arteriosclerosis obliterans 4) Patient has a history of allergy to extracorporeal circulation therapy. 5) Patient who received hemodiafiltration within two weeks before enrollment. 6) Patient who has participated in another drug or medical device clinical study in one month before consent. 7)Patient who has been judged to be unsuitable for participation in the study by the investigator 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