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Correlation of Hyperghrelinemia With Carotid Artery Intima-Media Thickness in Children With Prader-Willi Syndrome

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Samsung Medical Center

Status

Completed

Conditions

Obesity
Prader Willi Syndrome

Study type

Observational

Funder types

Other

Identifiers

NCT00474643
2006-06-043

Details and patient eligibility

About

Prader-Willi syndrome (PWS) is a genetic disorder characterized by childhood-onset obesity and endocrine dysfunction that leads to cardiovascular disability and early death within the first 3 decades of life.To assess the significance of risk factors for future disabilities, carotid artery intima-media thickness (IMT) was measured and correlated with known atherosclerotic risk factors in 27 children with PWS and 24 age-, sex-, and body mass index (BMI)-adjusted controls.

Full description

Main outcome measures: Correlation of IMT with age, standard deviation score of BMI (BMI-SDS), high-density lipoprotein cholesterol (HDL), low-density lipoprotein cholesterol (LDL), C-reactive protein, HOMA-IR and ghrelin.

Enrollment

51 patients

Sex

All

Ages

1 to 18 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Prader Willi syndrome
  • Children with obesity

Exclusion criteria

  • Acute illness
  • On regular medications except growth hormone

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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