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A Cohort Study of Precocious Puberty in Girls in Western China

A Cohort Study of Precocious Puberty in Girls in Western China

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112204
Enrollment
Unknown
Registered
2025-11-11
Start date
2025-07-22
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Precocious puberty

Interventions

Case series:None

Sponsors

The Second Affiliated Hospital of Xi’an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
5 Years to 10 Years

Inclusion criteria

Inclusion criteria: 1. Clinical manifestations and ancillary examinations meet the diagnostic criteria outlined in the Guidelines for the Diagnosis and Treatment of Precocious Puberty; 2. Female patients; 3. Guardians voluntarily sign the informed consent form. 4.Girls with central precocious puberty exhibit basal serum LH levels reaching pubertal thresholds (LH > 3.0–5.0 mIU/ml) or demonstrate a positive GnRH stimulation test. Those with incomplete precocious puberty show a negative GnRH stimulation test result.

Exclusion criteria

Exclusion criteria: 1. Concurrent central nervous system abnormalities; 2. Presence of skeletal, cutaneous or other systemic malformations, distinctive facial features, or family history of precocious puberty; 3. Concurrent malignant tumours, intellectual disability, short stature, or other genetic metabolic disorders; 4. History of prolonged corticosteroid use; 5. Presence of liver, thyroid, or renal disease; 6. Diagnosis of peripheral precocious puberty; 7. Initiation of treatment following confirmed diagnosis of precocious puberty.

Design outcomes

Primary

MeasureTime frame
melatonin;Perfluoroalkyl and polyfluoroalkyl substances;Follicle-stimulating hormone;Luteinising hormone;Estrogen;

Countries

China

Contacts

Public ContactJing Zhou

The Second Affiliated Hospital of Xi’an Jiaotong University

emily.34@163.com+86 177 4902 2902

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026