Evaluation of insulin resistance in obese children and adolescents referred to a paediatric obesity outpatient clinic: a follow up study.
Completed
- Conditions
- Obesitasinsulin resistance10018424
- Registration Number
- NL-OMON39352
- Lead Sponsor
- Sint Antonius Ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 89
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
Oral objection of subject and/or parents/caregivers for use of clinical data.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Main study parameters/endpoints:<br /><br>Primary endpoint is the HOMA-IR measured between 2-5 years after diagnosis of<br /><br>insulin resistance.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary endpoints are BMI, FPG, T2DM and quality of life between 2-5 years<br /><br>after diagnosis of insulin resistance</p><br>