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NCT06254768Recruiting

Use of Continuous Glucose Monitors in Children and Adolescents With Obesity

Source: ClinicalTrials.gov · Last updated 12 Feb 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Study type
Interventional
Enrollment
30 (estimated)
First submitted
27 Feb 2023
Start date
17 Jan 2023
Primary completion date
Mar 2024
Lead sponsor
University of California, Los Angeles
Diseases
Obesity
NCT number
NCT06254768

What you commit to

  • Study type: Interventional
  • Planned participants: 30
  • From 17 Jan 2023 to the primary completion date, Mar 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous diagnosis of Prader Willi Syndrome or hypothalamic obesity
  • Previous or planned bariatric surgery
  • Current use of medication that impacts weight

Lab values

  • Hemoglobin A1c \>6.5 %

Other

  • Intellectual disability

Who the study is looking for

  • Age 10-21 years BMI \>95th percentile

Age in the registry: 10 years to 21 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Pediatric Endocrinology Division, University of California
Coordinator of this site? Confirm its status
Los AngelesUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.