About this trial
The main objective of this study is to evaluate the effect of fully automated closed-loop glucose control on renal tissue oxygenation among people with type 2 diabetes and chronic kidney disease.
This is a single-center, open-label parallel design study that will compare 26 weeks of fully-automated closed-loop glucose control with standard insulin therapy and continuous glucose monitoring, following a run-in period. A total of up to 76 adults with type 2 diabetes and chronic kidney disease will be recruited through outpatient diabetes and nephrology clinics.
The primary outcome is renal tissue oxygenation measured using blood oxygenation level-dependent magnetic resonance imaging at 26 weeks. Other key outcomes include glycated hemoglobin at 26 weeks and time spent with glucose levels within and above the target glucose range (3.9-10.0mmol/L). Other glycemic and renal outcomes (including renal function) will also be assessed, as well as patient-reported outcome measures using validated questionnaires. Safety evaluations include severe hypoglycemic episodes and other adverse and serious adverse events.
Eligibility criteria
Qualifiers
Informed consent signed by the subject
Age 18 years and older
Type 2 diabetes diagnosed for at least 12 months
Treatment with insulin therapy for at least 6 months
Disqualifiers
Type 1 diabetes
Current use of insulin pump
Current use of any closed-loop system
Alternative cause of CKD according to medical records such as polycystic kidney disease, glomerulonephritis, congenital urogenital tract diseases, etc.
Trial design
Treatments tested in this trial
- CamAPS HX
- Standard insulin therapy with CGM
Treatment groups
Locations
2Sponsors and collaborators
Heba Al-Alwan
Lead sponsor
Centre Hospitalier Universitaire Vaudois
Sponsor institution
Swiss National Science Foundation
Collaborator
Institute of Primary Health Care (BIHAM), Switzerland
Collaborator