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Use of Continuous Glucose Monitors in Children and Adolescents With Obesity

University of California, Los Angeles · NCT06254768

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 10–21 · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
30
US sites recruiting
1
Study start
January 17, 2023
Record last updated
February 12, 2024

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

To study if continuous glucose monitors are feasible for use in children and adolescents with obesity.

Being studied: Continuous glucose monitor

Conditions: Pediatric Obesity

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full 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

Recruiting US locations

  • Pediatric Endocrinology Division, University of California

    Los Angeles, CA 90025

    Site contact: Sri Nikhita Chimatapu · 917-741-4080 · schimatapu@mednet.ucla.edu

Study contacts (from the official record)

  • Sri Nikhita Chimatapu, MD · 9177414080 · schimatapu@mednet.ucla.edu
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Use of Continuous Glucose Monitors in Children and Adolescents… (NCT06254768) | Bored Studies