Overview

Dianeal, Extraneal, Nutrineal (D-E-N) Versus Dianeal Only in Diabetic Continuous Ambulatory Peritoneal Dialysis (CAPD) Patients

Status:
Completed
Trial end date:
2011-07-01
Target enrollment:
0
Participant gender:
All
Summary
Primary Objective: To demonstrate that use of glucose sparing prescriptions, Dianeal, Extraneal, Nutrineal (D-E-N) versus Dianeal only, in diabetic (Type 1 and Type 2) Continuous Ambulatory Peritoneal Dialysis (CAPD) patients leads to improved metabolic control as measured by the magnitude of change from the baseline value in the HbA1c levels. Secondary Objectives: To demonstrate that use of glucose-sparing Peritoneal Dialysis solutions (D-E-N versus Dianeal only) in diabetic (Type 1 and Type 2) CAPD patients leads to lower glycemic-control medication requirements, decreased incidence of severe hypoglycemic events requiring medical intervention, improved metabolic control, nutritional status, and Quality of Life.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Baxter Healthcare Corporation
Treatments:
Icodextrin
Criteria
Inclusion Criteria:

1. Male or Female patients 18 years of age or older

2. Diagnosis of ESRD [Glomerular Filtration Rate (GFR) ≤ 15 mL/min]

3. CAPD using only Dianeal, at least 1 exchange of 2.5% or 4.25% dextrose/day, no
prescribed dry time

4. Diabetes Mellitus (Type 1 and 2)

5. HbA1c > 6.0% but ≤ 12.0%

6. Blood hemoglobin ≥ 8.0 g/dL, but ≤ 13.0 g/dL

7. Total Kt/V ≥ 1.7

Exclusion Criteria:

1. Blood Urea Nitrogen (BUN) > 95 mg/dL

2. Exposure to Extraneal within 60 days of Screening

3. Mean Arterial Pressure (MAP) ≥ 125 mm Hg, or volume depleted (MAP < 77mm Hg) at
Screening

4. Peritonitis, exit-site or tunnel infection treated with antibiotics within last 30
days

5. Cardiovascular event within the last 30 days

6. Ongoing clinically significant congestive heart failure [New York Heart Association
(NYHA) class III or IV]

7. Allergy to starch-based polymers, glycogen storage disease or isomaltose/maltose
intolerance

8. Receiving rosiglitazone maleate