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The efficacy and safety of long-acting growth hormone in improving final adult height in girls with rapid-progressing central precocious puberty or rapid-progressing puberty and advanced bone age:an observational study

The efficacy and safety of long-acting growth hormone in improving final adult height in girls with rapid-progressing central precocious puberty or rapid-progressing puberty and advanced bone age:an observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126101
Enrollment
Unknown
Registered
2026-06-03
Start date
2026-06-15
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Advanced bone age with rapid progression central precocious puberty

Interventions

GnRHa plus long-acting growth hormone (LAGH) combination group:None
GnRHa monotherapy group:None

Sponsors

Tongji Hospital, Tongji Medical College ,Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.Girls meeting all three of the following criteria: (1). Diagnostic criteria for Rapid progression CPP or EFP: Rapid progression CPP: 1). Breast development before age 7.5 or menarche before age 10; 2). Pelvic ultrasound showing enlarged uterine and ovarian volumes, with multiple ovarian follicles >=4mm in diameter; 3). GnRH stimulation test shows LH peak >=5.0 U/L with LH/FSH peak ratio >=0.6 or basal LH >=3 U/L (stimulation test not required for menarcheal cases); 4). Bone age exceeds chronological age by >=1 year; 5). Accelerated linear growth with annual growth rate exceeding that of healthy age-matched children; 6). Rapid progression through pubertal stages, with short intervals (=4mm in diameter visible in the ovaries; 3). GnRH stimulation test shows LH peak >=5.0 U/L with LH/FSH peak ratio >=0.6 or basal LH >=3 U/L (stimulation test not required in menstruating individuals). 4). Bone age exceeds chronological age by >=1 year; 5). Accelerated linear growth with annual growth rate exceeding that of healthy age-matched children; 6). Rapid progression through pubertal stages, with short intervals (= 12 years;

Exclusion criteria

Exclusion criteria: 1.Exclude individuals meeting any of the following criteria: Organic central precocious puberty, such as central precocious puberty caused by various intracranial tumours; 2.Peripheral precocious puberty converted to central precocious puberty, such as McCune-Albright syndrome, congenital adrenal hyperplasia, etc.; 3.Presence of contraindications for growth hormone use, such as diabetes mellitus, active tumours, etc.; 4.Concurrent conditions causing growth impairment or short stature, such as growth hormone deficiency (GHD), small for gestational age (SGA), idiopathic short stature (ISS), Turner syndrome, hypothyroidism, or short stature associated with other severe chronic diseases (e.g., cardiac insufficiency, hepatic or renal insufficiency, chronic inflammatory bowel disease); 5. Receipt of any GnRHa or GH therapy within the six months preceding the baseline period.

Design outcomes

Primary

MeasureTime frame
FAH SDS-PAH (pre-treatment) SDS;

Secondary

MeasureTime frame
?PAH SDS (difference in PAH SDS before and after treatment);FAH-THt;

Countries

China

Contacts

Public Contactye feng

Tongji Hospital, Tongji Medical College ,Huazhong University of Science and Technology

doctoryf@126.com+86 27 83662640

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026