Obesitas insulin resistance
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Signed informed consent. The need for informed consent is waived in case parents/caregivers and subjects during the visit to the outpatient clinic did not make an objection orally against the use of their clinical data. In the latter case, routinely collected clinical and laboratory data will be used only.
Exclusion criteria
Exclusion criteria: Oral objection of subject and/or parents/caregivers for use of clinical data.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main study parameters/endpoints: Primary endpoint is the HOMA-IR measured between 2-5 years after diagnosis of insulin resistance. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints are BMI, FPG, T2DM and quality of life between 2-5 years after diagnosis of insulin resistance | — |
Countries
Netherlands