Use of a Bimodal Solution for Peritoneal Dialysis
End Stage Renal Disease
About this trial
This is an interventional treatment trial for End Stage Renal Disease focused on measuring dialysis solutions, renal replacement therapy, peritoneal dialysis, bimodal solution, glucose sparing therapy
Eligibility Criteria
Inclusion Criteria:
- Be able to provide informed consent
- Age greater than 18 years
- Be stable Automated Peritoneal Dialysis (APD) patients for at least 6 weeks
Be APD patients who;
- Can be managed with an icodextrin long dwell AND
- Will use 4.25% and/or a 2.5% solution for at least one exchange overnight in at least 5 out of 7 days
- Have residual urine volume <800 ml/24 hours
- Long dwell must be or patient must tolerate at least an 8-10 hr long dwell.
Exclusion Criteria:
- Scheduled Transplant in the next 1 year
- Life expectancy < 3 mo (estimated by physician)
- Participating in other trial that could influence outcome of this trial
- Known icodextrin allergy
- Currently using non-Baxter PD solutions
- Systolic blood pressure < 90 mm Hg on more than three occasions during a seven day period, despite discontinuation of non-essential anti-hypertensives
Supplementary Exclusion Criteria (post Run-in phase):
1) Unsuccessfully completed 1 week run-in phase. Defined as:
- Not using bimodal solution on 7 consecutive days during the run-in
- Not tolerating the increased UF anticipated with the bimodal solution. Tolerating defined as:
i) Blood pressure drop below 90/50 on more than three occasions during a seven day period that cannot be corrected by reducing anti-hypertensives or other simple measures ii) Intolerable feeling of fullness with the bimodal solution iii) Allergic reaction (although all patients have already been exposed to icodextrin)
Sites / Locations
- London Health Sciences Centre, South Street Hospital, Peritoneal Dialysis Unit
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
bimodal solution
icodextrin
200 mls of 30% glucose in sterile water is added by the patient to the usual icodextrin day dwell, to create the bimodal solution intraperitoneally
200 mls of icodextrin is added by the patient to the usual icodextrin day dwell