Use of Continuous Glucose Monitors in Children and Adolescents With Obesity
Recruiting
N/A
Interventional Study
Pediatric Obesity
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 10 – 21
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 30 (estimated)
- Sponsor
- University of California, Los Angeles · Other
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About This Trial
To study if continuous glucose monitors are feasible for use in children and adolescents with obesity.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age 10-21 years BMI \>95th percentile
Exclusion Criteria:
* Previous diagnosis of Prader Willi Syndrome or hypothalamic obesity
* Intellectual disability
* Previous or planned bariatric surgery
* Hemoglobin A1c \>6.5 %
* Current use of medication that impacts weight
Contacts