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Active not recruitingPhase 4

Use of Liraglutide in Children Aged 6 to 12 Years With Severe Obesity

Efficacy, Metabolic and Cardiovascular Effects of Liraglutide in Children Aged 6-12 Years With Severe Obesity: A Randomized Controlled Trial With Advanced Echocardiographic Assessment

Asset

Liraglutide

Subcutaneous · GLP-1 agonist

Listed sites

1

Recruiting sites

Enrollment

30

estimated

Study population

Obesity / overweight

Key I/E criterion

Age 6-12

Primary endpoint

BMI, change

Footprint

Where this trial recruits

Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

NCT IDNCT07590219
Org study ID74225723.4.0000.0068

Timeline

Milestones

Study start2024-03-30actual
Study first posted2026-05-15actual
Last update posted2026-05-15actual
Primary completion2027-04estimated (month precision)
Study completion2028-04estimated (month precision)

Assets

Investigational agents

Study populations

Who this study enrolls

Obesity / overweight

Eligibility

Who can enroll

Minimum age6 Years
Maximum age12 Years
SexAll
Healthy volunteersNot accepted

Inclusion criteria

Children aged 6-12 years
BMI Z-score ≥ +3
Previous unsuccessful lifestyle intervention

Exclusion criteria

Severe chronic diseases
Cardiac disease
Dermatological contraindication
Use of interfering medications

Endpoints (9)

What's being measured

Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.

Coverage by outcome category

Cardiometabolic biomarkers
4
Glycemic / diabetes
2
Other (unclassified)
2
Weight & body composition
1

Weight & body composition

1 endpoint
Primary/protocol endpoint

Change in Body Mass Index (BMI)

Time frame:6 months

BMI, change

change from baseline, improvement

Glycemic / diabetes

2 endpoints
Secondary/protocol endpoint

Change in fasting plasma glucose

Time frame:Baseline to 6 months

Fasting glucose, change

change from baseline, improvement

LOINC 1558-6

Secondary/protocol endpoint

Change in fasting insulin levels

Time frame:6 months

change from baseline, improvement

Cardiometabolic biomarkers

4 endpoints
Secondary/protocol endpoint

Change in triglyceride levels

Time frame:6 months

Triglycerides, change

change from baseline, improvement

LOINC 2571-8

Secondary/protocol endpoint

Change in total cholesterol levels

Time frame:6 months

Total cholesterol, change

change from baseline, improvement

LOINC 2093-3

Secondary/protocol endpoint

Change in HDL cholesterol levels

Time frame:6 months

HDL-C, change

change from baseline, improvement

LOINC 2085-9

Secondary/protocol endpoint

Change in LDL cholesterol levels

Time frame:6 months

LDL-C, change

change from baseline, improvement

LOINC 13457-7

Other (unclassified)

2 endpoints
Secondary/protocol endpoint/low confidence

Change in left ventricular global longitudinal strain (LV-GLS) measured by two-dimensional speckle-tracking echocardiography

Time frame:6 months

change from baseline, improvement

Secondary/protocol endpoint/low confidence

Change in left atrial reservoir strain (LASr) measured by two-dimensional speckle-tracking echocardiography

Time frame:6 months

change from baseline, improvement

Publications (12)

Bibliography

Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.

Registry references + supporting bibliography

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 1, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.