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Use of a Bimodal Solution for Peritoneal Dialysis

Phase 2
Completed
Conditions
End Stage Renal Disease
Interventions
Drug: bimodal solution
Registration Number
NCT01242904
Lead Sponsor
Lawson Health Research Institute
Brief Summary

Peritoneal dialysis (PD) is the method of renal replacement therapy used by close to 200,000 end stage renal disease patients worldwide to help replace the functions that are no longer performed by their kidneys. An important advantage of PD is it offers an alternative to hemodialysis that can be safely performed by patients in their own homes. In PD, the peritoneal membrane that lines the abdomen acts as a dialyzer that allows the transfer of solutes and water between the membrane capillaries and a dialysis solution that is infused into the peritoneal cavity. PD dialysis solutions typically require high concentrations of glucose to adequately perform these functions. Over time the continued exposure of the peritoneal membrane to high concentrations of glucose can permanently damage the membrane. Icodextrin is a polyglucose molecule that has been developed for use in PD solutions that does not harm the peritoneal membrane. However, its use can lead to inadequate fluid removal. Recent research has focused on finding a PD solution, or combination of solutions, that will maximize the removal of toxic substances and metabolites while maintaining regulation of fluid and electrolyte balance in the body. A bimodal solution that combines glucose and icodextrin has been shown in observational studies to be effective and safe. The investigators propose a randomized, controlled, blinded study that will determine the effectiveness and safety of this bimodal fluid in a Canadian PD population. The investigators hypothesize that the use of the bimodal solution during the long (day) dwell will lead to an improvement in 24 hour ultrafiltration efficiency as compared to usual care using icodextrin for the long dwell.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
36
Inclusion Criteria
  1. Be able to provide informed consent

  2. Age greater than 18 years

  3. Be stable Automated Peritoneal Dialysis (APD) patients for at least 6 weeks

  4. Be APD patients who;

    1. Can be managed with an icodextrin long dwell AND
    2. Will use 4.25% and/or a 2.5% solution for at least one exchange overnight in at least 5 out of 7 days
  5. Have residual urine volume <800 ml/24 hours

  6. Long dwell must be or patient must tolerate at least an 8-10 hr long dwell.

Exclusion Criteria
  1. Scheduled Transplant in the next 1 year
  2. Life expectancy < 3 mo (estimated by physician)
  3. Participating in other trial that could influence outcome of this trial
  4. Known icodextrin allergy
  5. Currently using non-Baxter PD solutions
  6. 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:
  1. Not using bimodal solution on 7 consecutive days during the run-in
  2. 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)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
bimodal solutionbimodal solution200 mls of 30% glucose in sterile water is added by the patient to the usual icodextrin day dwell, to create the bimodal solution intraperitoneally
icodextrinicodextrin200 mls of icodextrin is added by the patient to the usual icodextrin day dwell
Primary Outcome Measures
NameTimeMethod
net ultrafiltration efficiency in mL/gCalculated at baseline and at the end of the 6 week intervention period

Ultrafiltration Efficiency (UFE): UFE is defined as the amount of 24 hour net Ultrafiltration (UF) obtained for every gram of carbohydrate absorbed from the dialysis solution.

1. 24-hour net ultrafiltration (in mL) is recorded automatically by the Automated Peritoneal Dialysis (APD) cycler.

2. Carbohydrate absorption is determined by calculating the difference (in grams) between the amount of glucose (measured by lab analysis) in the 24 hr peritoneal effluent, and the amount of glucose in the patient's dialysis prescription.

3. UFE will be calculated in mL/g (ie a divided by b)

Secondary Outcome Measures
NameTimeMethod
24-hour absolute total carbohydrate absorptionCalculated at baseline and at the end of the 6 week intervention period

This will include both glucose and icodextrin absorption.

24-hour urine volumeCalculated at baseline and at the end of the 6 week intervention period
24-hour net sodium removal (in both peritoneal effluent and urine)Calculated at baseline and at the end of the 6 week intervention period
Volume measures as calculated by bioimpedance analysisCalculated at baseline and at the end of the 6 week intervention period
WeightCalculated at baseline and at the end of the 6 week intervention period

Used as an indicator of fluid retention

Mean and pulse arterial pressureCalculated at baseline and at the end of the 6 week intervention period
Number of anti-hypertensive agentsCalculated at baseline and at the end of the 6 week intervention period
Renal (urine) solute clearance (Sodium, Urea, Creatinine)Calculated at baseline and at the end of the 6 week intervention period
Peritoneal effluent solute clearance (Sodium, Urea, Creatinine)Calculated at baseline and at the end of the 6 week intervention period

Trial Locations

Locations (1)

London Health Sciences Centre, South Street Hospital, Peritoneal Dialysis Unit

🇨🇦

London, Ontario, Canada

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