Peritoneal Dialysis Versus Haemodialysis
Not Applicable
Completed
- Conditions
- Hemodialysis
- Interventions
- Procedure: HaemodialysisProcedure: Peritoneal dialysis
- Registration Number
- NCT00752583
- Lead Sponsor
- University Hospital, Ghent
- Brief Summary
Study in order to quantify toxin removal during dialysis
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 25
Inclusion Criteria
- Substudy 1: includes new starting dialysis patients on peritoneal dialysis PD or haemodialysis HD
- Substudy 2: stabile haemodialysis patients and peritoneal dialysis patients. Patients will be matched for gender, time on dialysis, diabetes, renal function at the start of dialysis.
- Substudy 3: patients on CAPD (continuous ambulant PD) or CCPD (continuous cyclic PD).
Exclusion Criteria
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description 2 Haemodialysis Haemodialysis 1 Peritoneal dialysis Peritoneal dialysis
- Primary Outcome Measures
Name Time Method Registration of toxin removal efficiency After 1 week and after 1, 3, 6, 9, 12, 18 and 24 months
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University Hospital Ghent
🇧🇪Ghent, Belgium