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Magnetic Resonance Imaging Assessment of Multiorgan Health in Obesity

Impact of Weight Loss Interventions on Multiorgan Health, Detected by Quantitative MRI, in Children and Young People With Severe Obesity.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07702825
Acronym
FIT-YOUNG
Enrollment
30
Registered
2026-07-14
Start date
2026-03-06
Completion date
2028-01-01
Last updated
2026-07-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Childhood Obesity

Keywords

Obesity, GLP1 receptor agonist, MRI Body composition

Brief summary

The goal of this study is to quantify the body composition and organ fat distribution changes with obesity interventions in adolescents with severe obesity. The main question the investigators aim to answer is if there is improvement in organ health with weight loss intervention. The investigators will be comparing the degree of these changes between children being treated with GLP1 receptor agonists in addition to lifestyle changes and those managed with lifestyle changes alone. Participants will undergo MRI body composition at baseline and after 9 months.

Interventions

None listed

Sponsors

Alder Hey Children's NHS Foundation Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Age 12 to \<18 years at the time of enrolment * BMI \>99.6th centile or \>2.67 SDS * Informed consent from parent(s) (or person with parental responsibility) and assent from the child or young person for participants aged less than 16 years (or) * Informed consent from the participant if aged ≥ 16 years.

Exclusion criteria

* Body weight above upper limit of the scanner (\>250 kilograms) * Needs general anaesthesia for the MRI scanning * Any contraindications for MRI- Metal implants/claustrophobia * Previous use of GLP-1 receptor agonist * Refusal to consent or refusal to assent from a competent older adolescent.

Design outcomes

Primary

MeasureTime frameDescription
Change in Liver fat measured using quantitative MRIFrom enrollment to 9 monthsChange in liver fat content from baseline to follow-up, quantified using MRI-derived proton density fat fraction (PDFF).

Secondary

MeasureTime frameDescription
Changes to body composition assessed by MRIBaseline to 9 monthsChange from baseline in Visceral adipose tissue(VAT) and Subcutaneous adipose tissue (VAT) measured in cm2 assessed by quantitative MRI
Change in pancreatic fat assessed by MRI.Baseline to 9 monthsChange from baseline in pancreatic fat measured as proton density fat fraction (%) assessed by quantitative MRI.
Changes in biochemical parameters-fasting glucose9 monthsChanges from baseline in fasting glucose measured in mmol/l
Changes in biochemical parameters-HbA1C9 monthsChange from baseline in HbA1C measured in mmol/mol

Countries

United Kingdom

Contacts

CONTACTAnand Ramakrishnan, MD (Ped), MSc (Diab), PhD endo
senthil.senniappan@alderhey.nhs.uk+44 01512525956
CONTACTAnand Ramakrishnan, MBBS, MD, MRCPCH, DipUKMP
anand.ramakrishnan@alderhey.nsh.uk07404613764

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 15, 2026