A multi-institutional retrospective observational study on the clinical safety and efficacy of Central Dialysis fluid Delivery System (CDDS)
Not Applicable
- Conditions
- chronic renal failure
- Registration Number
- JPRN-UMIN000040141
- Lead Sponsor
- Toray Medical Company Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Not provided
Exclusion Criteria
1)Patients who use continuous ambulatory peritoneal dialysis (CAPD) together during the clinical data collection period 2)Patients who are judged inappropriate for inclusion in this study by the investigators
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Accuracy of fluid removal Incidence of adverse events and malfunctions
- Secondary Outcome Measures
Name Time Method