OTHERClinicalTrials.govClinical trialNot yet recruiting
Biomarker Panel for PCOS-Associated Liver Steatosis in Adolescent Girls (COMPASS-pedPCOS)
Official record
- Identifier
NCT07731373- Recruiting locations
country
Turkey (Türkiye)- Interventions studied
- Extended Serum Biomarker and Hormonal PanelLiver Elastography with Controlled Attenuation ParameterTargeted Genotyping of PNPLA3 rs738409 and HSD17B13 rs72613567
- Lead sponsor
- Kayseri City Hospital
- Target enrolment
- 150 participants
- Study type
- OBSERVATIONAL
- Phase
- Not provided in the official record
- Status
- Not yet recruiting
- First posted
- Jul 28, 2026
- Last updated on the registry
- Jul 30, 2026
- Age
- 10 Years – 18 Years
- Sex
- FEMALE
- Study contact
- The official record lists a study contact. Contact details are published there and are intentionally not copied to this page.
- Eligibility criteria
Reproduced verbatim from the official record. Eligibility is decided by the study team, never by this page.
Inclusion Criteria: * Female, aged 10 to 18 years, with written informed consent from a parent or legal guardian and written assent from the child. * Group 1 (PCOS with obesity): both hyperandrogenism and oligo-anovulation required, based on adolescent-adapted Rotterdam criteria; body mass index at or above the 95th percentile. * Group 2 (Obesity control): body mass index at or above the 95th percentile, without features of PCOS, matched to Group 1 for age and body mass index. * Group 3 (Healthy control): healthy normal-weight girls (body mass index between the 5th and 84th percentile) without chronic disease, hyperandrogenism, or menstrual irregularity. Exclusion Criteria: * Known acute or chronic liver disease (including viral, autoimmune, or Wilson disease) or use of hepatotoxic medication. * Endocrine disorders or secondary hyperandrogenism, including Cushing syndrome, hypothyroidism, uncontrolled diabetes mellitus, congenital adrenal hyperplasia, androgen-secreting tumour, or hyperprolactinaemia. * Syndromic or monogenic obesity (including Prader-Willi syndrome, Bardet-Biedl syndrome, Alström syndrome, MC4R or LEP variants) or a known genetic disorder. * Use of relevant or hepatotoxic medication within the preceding three months, including corticosteroids, metformin, oral contraceptives, valproic acid, or antiandrogens. * Pregnancy or regular alcohol use. * Refusal of consent or assent.
- Indexed under
- Liver Cancer
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