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

No treatment groups listed

Locations

1
Department of Medicine and Therapeutics, The Chinese University of Hong Kong Hong Kong Hong Kong

Sponsors and collaborators

Elaine Chow

Lead sponsor

Chinese University of Hong Kong

Sponsor institution

Medtronic MiniMed, Inc.

Collaborator