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Use of a Bimodal Solution for Peritoneal Dialysis

Primary Purpose

End Stage Renal Disease

Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
bimodal solution
icodextrin
Sponsored by
Lawson Health Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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)

Sites / Locations

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

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

bimodal solution

icodextrin

Arm Description

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

Outcomes

Primary Outcome Measures

net ultrafiltration efficiency in mL/g
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. 24-hour net ultrafiltration (in mL) is recorded automatically by the Automated Peritoneal Dialysis (APD) cycler. 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. UFE will be calculated in mL/g (ie a divided by b)

Secondary Outcome Measures

24-hour absolute total carbohydrate absorption
This will include both glucose and icodextrin absorption.
24-hour urine volume
24-hour net sodium removal (in both peritoneal effluent and urine)
Volume measures as calculated by bioimpedance analysis
Weight
Used as an indicator of fluid retention
Mean and pulse arterial pressure
Number of anti-hypertensive agents
Renal (urine) solute clearance (Sodium, Urea, Creatinine)
Peritoneal effluent solute clearance (Sodium, Urea, Creatinine)

Full Information

First Posted
November 16, 2010
Last Updated
August 25, 2017
Sponsor
Lawson Health Research Institute
Collaborators
Baxter Healthcare Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT01242904
Brief Title
Use of a Bimodal Solution for Peritoneal Dialysis
Official Title
Randomized Controlled Trial of Bimodal Solution for Peritoneal Dialysis: 24-Hour UF Efficiency Using Bimodal PD Solutions During the Long Dwell
Study Type
Interventional

2. Study Status

Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
September 30, 2010 (Actual)
Primary Completion Date
February 28, 2015 (Actual)
Study Completion Date
February 28, 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lawson Health Research Institute
Collaborators
Baxter Healthcare Corporation

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End Stage Renal Disease
Keywords
dialysis solutions, renal replacement therapy, peritoneal dialysis, bimodal solution, glucose sparing therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
36 (Actual)

8. Arms, Groups, and Interventions

Arm Title
bimodal solution
Arm Type
Experimental
Arm Description
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
Arm Title
icodextrin
Arm Type
Active Comparator
Arm Description
200 mls of icodextrin is added by the patient to the usual icodextrin day dwell
Intervention Type
Drug
Intervention Name(s)
bimodal solution
Intervention Description
200 mL of 30% glucose infused into the abdomen by the patient each morning for 6 weeks, added to the daytime dwell of approximately 2000 mL icodextrin that has been infused by the cycler
Intervention Type
Drug
Intervention Name(s)
icodextrin
Intervention Description
200 mL of icodextrin infused into the abdomen by the patient each morning for 6 weeks, added to the daytime dwell of approximately 2000 mL icodextrin that has been infused by the cycler
Primary Outcome Measure Information:
Title
net ultrafiltration efficiency in mL/g
Description
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. 24-hour net ultrafiltration (in mL) is recorded automatically by the Automated Peritoneal Dialysis (APD) cycler. 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. UFE will be calculated in mL/g (ie a divided by b)
Time Frame
Calculated at baseline and at the end of the 6 week intervention period
Secondary Outcome Measure Information:
Title
24-hour absolute total carbohydrate absorption
Description
This will include both glucose and icodextrin absorption.
Time Frame
Calculated at baseline and at the end of the 6 week intervention period
Title
24-hour urine volume
Time Frame
Calculated at baseline and at the end of the 6 week intervention period
Title
24-hour net sodium removal (in both peritoneal effluent and urine)
Time Frame
Calculated at baseline and at the end of the 6 week intervention period
Title
Volume measures as calculated by bioimpedance analysis
Time Frame
Calculated at baseline and at the end of the 6 week intervention period
Title
Weight
Description
Used as an indicator of fluid retention
Time Frame
Calculated at baseline and at the end of the 6 week intervention period
Title
Mean and pulse arterial pressure
Time Frame
Calculated at baseline and at the end of the 6 week intervention period
Title
Number of anti-hypertensive agents
Time Frame
Calculated at baseline and at the end of the 6 week intervention period
Title
Renal (urine) solute clearance (Sodium, Urea, Creatinine)
Time Frame
Calculated at baseline and at the end of the 6 week intervention period
Title
Peritoneal effluent solute clearance (Sodium, Urea, Creatinine)
Time Frame
Calculated at baseline and at the end of the 6 week intervention period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arsh K Jain, MD
Organizational Affiliation
London Health Sciences Centre, Dept of Medicine, Victoria Campus, London Ontario
Official's Role
Principal Investigator
Facility Information:
Facility Name
London Health Sciences Centre, South Street Hospital, Peritoneal Dialysis Unit
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5W9
Country
Canada

12. IPD Sharing Statement

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Use of a Bimodal Solution for Peritoneal Dialysis

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