Actively Recruiting
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
Eligibility Criteria
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
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
Trial Site Locations
Total: 1 location
1
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Bologna, Bolgona, Italy, 40138
Actively Recruiting
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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