Continuous Glucose Monitoring (CGM) After Kidney Transplantation

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorBo Feldt-Rasmussen

About this trial

This study examines glucose levels measured by continuous glucose monitoring (CGM) in the immediate period following kidney transplantation among recipients with diabetes, without diabetes, and with pre-diabetes.

The primary objective is to analyse differences in mean sensor glucose between these three groups.

CGMs are applied to participants within 72 hours after kidney transplantation, with a total of 54 participants divided equally across the three groups (18 in each).

Secondary objectives include assessing additional glucose profile indices, adherence to relevant guidelines, changes in HbA1c, the impact of immunosuppression and steroid dosage, and beta cell function.

Eligibility criteria

Qualifiers

Written informed consent obtained before CGM application

Male or female; age: ≥18 years

Kidney transplantation

Disqualifiers

Unable to cooperate to CGM the first ten days after surgery

Allergic to plasters in CGM units

Combined kidney and liver or pancreatic transplantation

Graft loss/rejection within first 48 hours after transplantation

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

54 Participants
are grouped into 3 trial groups

Sponsors and collaborators

Bo Feldt-Rasmussen

Lead sponsor

Rigshospitalet, Denmark

Sponsor institution