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Recruiting Observational

Idiopathic Central Precocious Puberty and Associated Neurodevelopmental Syndromes and Pathologies: Evaluation of Frequency and Comparison of Diagnostic and Developmental Characteristics

NCT06720844 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2024-03-13
Last updated
2026-03-12

Condition(s) studied

Central Precocious Puberty (CPP)

Study summary

Observational, retrosopective, single-centre, non-profit study focused on the frequency of Central Precocious Puberty idiopathic, or associated to Neurodevelopmental Syndromes and Pathologies, and comparison of diagnostic and developmental characteristics of patients.

Eligibility

Sex
ALL
Min age
—
Max age
18 Years
Healthy volunteers
No
Inclusion Criteria: * Patients diagnosed with Central Precocious Puberty presenting an indication to undertake treatment with GnRH analogue: Appearance of secondary sexual characteristics (thelarche or gonadarche) before the age of 8 for females and 9 for males; Acceleration of the rate of statural growth and advancement of bone age one year older than the chronological age; LH peak \> 5 IU/L on GnRH test and a longitudinal uterine diameter \> 36 mm in females, with or without the appearance of endometrial rhyme; * Age at onset of entral Precocious Puberty between 2 and 8 years (females) or between 2 and 9 years (males); * Age at enrollment \< 18 years; * Follow-up of at least 12 months; * Obtaining informed consent from parents/legal guardian of peduatric patients. Exclusion Criteria: * Isolated telarche and/or pubarche; * Peripheral forms of precocious puberty; * Patients diagnosed with primary organic Central Precocious Puberty due to tumour- or non-tumour-causing hypothalamic lesions.

Primary outcome measure(s)

  • Frequency of diagnosis of idiopathic or syndromic Central Precocious Puberty — at baseline
    diagnosis of idiopathic or syndromic Central Precocious Puberty

Trial sites (1)

FacilityCityRegionStatus
IRCCS Azienda Ospedaliero-Universitaria di Bologna Bologna Bolgona Recruiting
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 NCT06720844 on ClinicalTrials.gov ↗ ← All trials in Italy