Assessment of the Accuracy of Continuous Glucose Sensors in People With Diabetes Undergoing Haemodialysis (ALPHA)
Diabetic Nephropathies, Type 1 Diabetes Mellitus, Chronic Kidney Diseases
About this trial
This is an interventional prevention trial for Diabetic Nephropathies focused on measuring Type 1 Diabetes Mellitus, Chronic Kidney Diseases
Eligibility Criteria
Inclusion Criteria:
- Adults >18 years of age
- Diabetes, with insulin treatment for over 6 months or on sulphonylureas
- Chronic kidney disease requiring haemodialysis three times per week
Exclusion Criteria:
- Pregnant or planning pregnancy
- Breastfeeding
- Enrolled in other clinical trials
- Have active malignancy or under investigation for malignancy
- Severe visual impairment
- Reduced manual dexterity
- Unable to participate due to other factors, as assessed by the Chief Investigators
Sites / Locations
- Imperial College London/NHS trust Renal Unit
Arms of the Study
Arm 1
Experimental
Dexcom G6 and Abbott Freestyle Libre
Participants will have a Dexcom G6 sensor and Abbott FreeStyle Libre sensor inserted in the abdomen and upper arm respectively. Participants will be asked to swipe the FreeStyle Libre reader across the sensor a minimum of every 8 hours. Participants will be asked to continue their usual regimen of self-monitoring capillary blood glucose (SMBG). During haemodialysis, a dialysis circuit blood sample will be drawn at 0 (pre-dialysis) 30, 60, 90, 120, 150, 180, 210 and 240 minutes and immediately after dialysis. Samples from the circuit will be analysed on the YSI glucose analyser. Participants will be asked to change the FreeStyle Libre sensors at day 14. The blinded CGM data will be uploaded at the time of each sensor change by the research team.