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Efficacy and safety of gonadotropin-releasing hormone analogues in the treatment of central precocious puberty: a retrospective cohort study

Efficacy and safety of gonadotropin-releasing hormone analogues in the treatment of central precocious puberty: a retrospective cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300068209
Enrollment
Unknown
Registered
2023-02-10
Start date
2023-02-01
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

central precocious puberty

Interventions

Group of patients treated with GnRHa:N/A
Group of patients receiving GnRHa combined with rhGH:N/A
Group of patients who did not receive or refused to receive GnRHa treatment:N/A

Sponsors

West China Second University Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosis of CPP, age 3.4 cm in length, ovarian volume > 1 mL and multiple follicles > 4 mm in diameter in girls; testicular volume >= 4 mL or testicular length diameter > 2.5 cm in boys; 6. Basal serum gonadotropin levels reaching to the levels of puberty with LH > 5.0 IU/L; 7. Serum gonadotropin level reaching to the levels of puberty, with GnRH stimulation test showing peak LH >= 5.0 U/L and peak LH/ peak FSH >= 0.6.

Exclusion criteria

Exclusion criteria: 1. Secondary CPP with a clear etiology, such as central nervous system abnormalities, congenital adrenocortical hyperplasia, McCune-Albright syndrome, primary hypothyroidism, familial male-limited precocious puberty; 2. Those with other conditions related to gonadal function, such as simple premature breast development; 3. Those with a combination of other conditions that may affect height, such as severe malnutrition, growth hormone deficiency, etc.; 4. Those who have been treated in an external hospital; 5. Those who have achieved final height (FH) at the time of first consultation; 6. Those with incomplete data on important covariates.

Design outcomes

Primary

MeasureTime frame
final height;final height - initial predicted adult height;final height - target height;

Secondary

MeasureTime frame
final height standard deviation score;

Countries

China

Contacts

Public ContactLingli Zhang

West China Second University Hospital, Sichuan University

zhanglingli@scu.edu.cn+86 181 8060 9021

Outcome results

None listed

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