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Effects of Liraglutide in obese children with Autism disorder

The clinical and chemical effects of Liraglutide in obese children with Autism disorder

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240119060733N1
Enrollment
20
Registered
2024-10-05
Start date
2024-02-20
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Condition 1: Obesity. Condition 2: Autism. Overweight and obesity Autistic disorder

Interventions

Intervention 1: Receiving Liraglutide (manufactured by Sinagene company under the brand name Melitide) as a subcutaneous injection at the rate of 3 mg per day for sixteen weeks (with 0.6 mg per day an

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 18 Years

Inclusion criteria

Inclusion criteria: Having Autism with the confirmation of a specialist doctor using diagnostic indicators Being obese (be above the 95th percentile of BMI for age and sex) Have been lost less than 5 kg in the last three months Age 12 - 18 years Completion of consent form by patients parents

Exclusion criteria

Exclusion criteria: Liver or kidney failure Type 1 diabetes A history of suicide attempts or the existence of suicidal thoughts in a person or relatives Having thyroid cancer, C-cell thyroid tumors, MEN tumors or a family history of these tumors

Design outcomes

Primary

MeasureTime frame
Changes in BMI. Timepoint: At the beginning of the study, at the end of the fourth week, at the end of the tenth week, and at the end of the sixteenth week. Method of measurement: Height is measured using a standard inelastic meter and weight is measured using a standard fixed scale, then BMI is calculated using the formula.;Changes in BMI Z scores. Timepoint: At the beginning of the study, at the end of the fourth week, at the end of the tenth week, and at the end of the sixteenth week. Method of measurement: Height is measured using a standard inelastic meter and weight is measured using a standard fixed scale, then BMI is calculated using the; Then Z score is calculated.

Secondary

MeasureTime frame
FBS. Timepoint: The beginning and end of the study. Method of measurement: Using standard measurement kits.;Anthropometric data. Timepoint: The beginning and end of the study. Method of measurement: Anthropometry is done with the help of an Bioimpedance analysis (BIA) made by Tanita company.;HOMA-IR. Timepoint: The beginning and end of the study. Method of measurement: Using standard measurement kits.;Blood Triglyceride (TG) level. Timepoint: The beginning and end of the study. Method of measurement: Using standard measurement kits.;LDL. Timepoint: The beginning and end of the study. Method of measurement: Using standard measurement kits.;HDL. Timepoint: The beginning and end of the study. Method of measurement: Using standard measurement kits.;HbA1C. Timepoint: The beginning and end of the study. Method of measurement: Using standard measurement kits.;Hip circumference. Timepoint: The beginning and end of the study. Method of measurement: Using a non-stretchable standard meter, the largest hip circumference is measured.;Waist circumference. Timepoint: The beginning and end of the study. Method of measurement: The smallest waist circumference is measured using a non-elastic standard meter.;Circumference around the neck. Timepoint: The beginning and end of the study. Method of measurement: With the help of a non-stretchable standard meter, the neck circumference is measured in a standing position under the ridge of the throat.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMorteza Ghasemi

Mashhad University of Medical Sciences

ghasemim4012@mums.ac.ir+98 51 3800 2000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026