Actively Recruiting
Use of Continuous Glucose Monitors in Children and Adolescents With Obesity
Led by University of California, Los Angeles · Updated on 2024-02-12
30
Participants Needed
1
Research Sites
71 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To study if continuous glucose monitors are feasible for use in children and adolescents with obesity.
CONDITIONS
Official Title
Use of Continuous Glucose Monitors in Children and Adolescents With Obesity
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 10 to 21 years
- Body mass index (BMI) greater than the 95th percentile for age
You will not qualify if you...
- Previous diagnosis of Prader Willi Syndrome or hypothalamic obesity
- Intellectual disability
- Previous or planned bariatric surgery
- Hemoglobin A1c greater than 6.5%
- Current use of medication that impacts weight
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Pediatric Endocrinology Division, University of California
Los Angeles, California, United States, 90025
Actively Recruiting
Research Team
S
Sri Nikhita Chimatapu, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
PREVENTION
Number of Arms
2
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