Clinical Trials Directory

Trials / Completed

CompletedNCT00567398

IMPENDIA- PEN VS Dianeal Only Improved Metabolic Control In Diabetic CAPD and APD Patients

Multi-center,Prospective, Randomized Trial ToDemonstrate Improved Metabolic Control of PEN VS Dianeal In Diabetic CAPD and APD Patients - The Impendia Trial

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
43 (actual)
Sponsor
Vantive Health LLC · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Primary Objective: To demonstrate that use of glucose sparing prescriptions (PEN vs Dianeal) in diabetic (Type 1 and Type 2) Continuous Ambulatory Peritoneal Dialysis (CAPD)and Automated Peritoneal Dialysis (APD) 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 PD solutions (PEN vs Dianeal) in diabetic (Type 1 and Type 2) CAPD and APD 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. In a subgroup of patients, the impact of glucose-sparing PD solutions (PEN vs Dianeal only) on abdominal fat and left ventricular (LV) structure and function will be assessed.

Conditions

Interventions

TypeNameDescription
DRUGDianealDianeal 1.5% Dextrose (1.38% Glucose), 2.5% Dextrose (2.27% Glucose), 4.25% Dextrose (3.86% Glucose)
DRUGPhysionealPhysioneal 40 or Physioneal 35
DRUGExtranealExtraneal - 7.5% Icodextrin
DRUGNutrinealNutrineal - 1.1% Amino Acids

Timeline

Start date
2008-04-01
Primary completion
2011-07-01
Completion
2011-07-01
First posted
2007-12-05
Last updated
2025-07-22
Results posted
2019-06-03

Locations

16 sites across 3 countries: Australia, Canada, New Zealand

Source: ClinicalTrials.gov record NCT00567398. Inclusion in this directory is not an endorsement.