About this trial
Assessment of performance (precision and accuracy) of Simplera™ CGM as compared with a gold standard reference laboratory method (YSI glucose) in diabetes patients on peritoneal dialysis with icodextrin
Eligibility criteria
Qualifiers
Type 1 or 2 diabetes mellitus for at least 3 months
On continuous ambulatory peritoneal dialysis (CAPD) or APD for at least 2 months
On icodextrin PD solutions for at least 1 month or planned for switching to icodextrin PD solutions within 3 months of screening
Male or female age ≥ 18 years old and ≤ 75 year old.
Disqualifiers
Poorly controlled diabetes mellitus with HbA1c>11%
Peritonitis within 1 month of screening
Planned for switching to hemodialysis or living donor transplant in the future 1 month
Currently pregnant, as demonstrated by a positive pregnancy test at screening for women of reproductive potential
Trial design
Treatments tested in this trial
- Continuous glucose monitoring system
Treatment groups
Locations
1Sponsors and collaborators
Elaine Chow
Lead sponsor
Chinese University of Hong Kong
Sponsor institution
Medtronic MiniMed, Inc.
Collaborator