CGM in Icodextrin PD

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorElaine Chow

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

Sponsors and collaborators

Elaine Chow

Lead sponsor

Chinese University of Hong Kong

Sponsor institution

Medtronic MiniMed, Inc.

Collaborator