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Starting soon Not applicable

SCUBE Proteins in Polycystic Ovary Syndrome (IPSOS)

NCT07396402 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2026-01-15
Last updated
2026-02-09

Condition(s) studied

Polycystic Ovary Syndrome (PCOS)Insulin Resistance

Investigational drug(s) / intervention(s)

Blood Sample Collection for SCUBE-1 and SCUBE-3 Measurement

Blood Sample Collection for SCUBE-1 and SCUBE-3 Measurement: Blood sample collection performed specifically for research purposes to measure circulating SCUBE-1 and SCUBE-3 levels using enzyme-linked immunosorbent assay (ELISA).

Study summary

This study investigates circulating levels of SCUBE-1 and SCUBE-3 proteins in women with polycystic ovary syndrome (PCOS) compared with healthy controls. Differences between normoinsulinemic and hyperinsulinemic PCOS subgroups will be evaluated, as well as correlations with clinical and metabolic parameters related to inflammation and cardiovascular risk.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
35 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Female subjects aged 18-35 years * Diagnosis of polycystic ovary syndrome (normoinsulinemic or hyperinsulinemic) * Availability of basal hormonal evaluation and oral glucose tolerance test * Healthy women for control group * Written informed consent Exclusion Criteria: * Pregnancy * History of cardiovascular disease * Diabetes mellitus or impaired glucose tolerance * Hypertension * Significant hepatic or renal disease * Other endocrine disorders * Neoplastic diseases * Psychiatric disorders * Autoimmune diseases * Shift work * Obesity * Refusal to sign informed consent

Primary outcome measure(s)

  • Circulating SCUBE-1 levels — At enrollment
    Comparison of SCUBE-1 plasma concentrations among normoinsulinemic PCOS, hyperinsulinemic PCOS, and healthy controls

Trial sites (1)

FacilityCityRegionStatus
Fondazione Policlinico Universitario Agostino Gemelli IRCCS Roma Italy
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07396402 on ClinicalTrials.gov ↗ ← All trials in Italy