Patients with end-stage renal disease on peritoneal dialysis
Conditions
Interventions
Group I
Patients treated with glucose-based dialysate, to whom PLP is not given (n=20).
Group II
Patients treated with glucose-based dialysate, to whom PLP is given (300mg/day, n=20)
Sponsors
Miyanomori Memorial Hospital
Nikko Memorial Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1, Patients who are aged above 18 2, Patients with chronic renal failure on peritoneal dialysis 3, Fully informed consent should be obtained
Exclusion criteria
Exclusion criteria: 1, Patients with heart failure of NYHAIII and IV
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| After starting PLP treatment, the concentrations of growth factors, chemical mediators and AGE in used dialysate will be regularly measured and those indices will be compared between dialysate before and after PLP treatment. | — |
Secondary
| Measure | Time frame |
|---|---|
| An appropriate daily dosage of PLP will be determined. | — |
Countries
Japan
Contacts
Public ContactSakurako Nakamura
Miyanomori Memorial Hospital Clinical nephrology
Outcome results
None listed