Actively Recruiting

Age: 0 - 18Years
All Genders
NCT06720844

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

Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2026-03-12

300

Participants Needed

1

Research Sites

165 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 0 - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with Central Precocious Puberty showing signs before age 8 (females) or 9 (males), including early secondary sexual characteristics, faster growth, and advanced bone age
  • LH peak greater than 5 IU/L on GnRH test and uterine diameter over 36 mm in females, with or without endometrial lining
  • Age at onset of puberty between 2 and 8 years for females, and between 2 and 9 years for males
  • Age under 18 years at enrollment
  • At least 12 months of follow-up after starting treatment
  • Informed consent obtained from parents or legal guardians for pediatric patients
Not Eligible

You will not qualify if you...

  • Presence of isolated thelarche or pubarche only
  • Peripheral forms of precocious puberty
  • Central Precocious Puberty caused by hypothalamic lesions from tumors or other organic causes

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Bologna, Bolgona, Italy, 40138

Actively Recruiting

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Research Team

F

Federico Baronio, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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