About this trial
Diabetes mellitus is a widespread disease with increasing prevalence worldwide. Patients with diabetes can develop multiple late complications such as neuropathy, retinopathy, nephropathy and cardiovascular comorbidities. So far, there are no reliable predictive tools or markers to estimate if, when and to what extent a patient with diabetes develops late complications. For the patients quality of life and for health economic reasons an improved risk assessment would be desirable. The prospective TUEDID study will characterize diabetic patients to look out for parameters the predict progression of diabetes and its complications.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
>18 years
Disqualifiers
no written informed consent
Trial population
People with or without diabetes who are treated at the University Hospital Tübingen
Trial design
Cohort
Other
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Glycemic control (blood glucose)
Assessed as fasting blood glucose and HbA1C
Glycemic control (HbA1C)
Assessed as fasting HbA1C
Other outcomes
Liver function
Parameters for liver function will be assessed (GOT, GPT, AP, Gamma-GT, Lipase, all \[U/l\])
Renal function
Parameters for renal function will be assessed (Creatinine, Urea, Cystatin C, all \[mg/dl\])
Glomerular filtration rate (GFR)
Glomerular filtration rate will be determined \[ml/min/1,73 m²\]
Lipid status
Parameters for evaluation of lipid status will be assessed (LDL, HDL, Cholesterol, triglycerides, all \[mg/dl\])
Sponsors and contacts
Click on the lead sponsor to view all of their trials.