Methods to determine the dialysis dose in clinical applicatio
- Conditions
- Z49Care involving dialysis
- Registration Number
- DRKS00000499
- Lead Sponsor
- Fresenius Medical Care Deutschland GmbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 1089
Inclusion Criteria
Adult haemodialysis patient
- Signed informed consent
- Physical and mental ability to participate in the study
- Double-needle dialysis
- Haemodialysis or on-line Haemodiafiltration
Exclusion Criteria
- Pregnancy in case of female patient
- Pace maker
- Implanted pump
- Major amputation of arm or leg
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Simultaneous determination of dialysis dose with 3 different methods (Kt/V_Dau, KtV_OCM, Kt/V_BCM) once in each haemodialysis patient
- Secondary Outcome Measures
Name Time Method Hydration status of haemodialysis patients by single BCM measurement