Actively Recruiting

Phase 3
Age: 4Years - 9Years
FEMALE
ID06510764

A Randomized Controlled Trial of Ziyin-Xiehuo Chinese Medicine Herbs Combined With Intradermal Acupuncture for the Treatment of Girl's Idiopathic Precocious Puberty With Yin Deficiency and Fire Hyperactivity

Led by Children's Hospital of Fudan University · Updated on 2026-03-16

170

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of traditional Chinese medicine combined with intradermal acupuncture on girls with idiopathic precocious puberty, a condition characterized by early onset of puberty without an identifiable cause. This phase 3 randomized controlled trial aims to determine if combining acupuncture point stimulation with herbal treatment can improve symptoms and prevent the condition from worsening. The study focuses on girls with mild to moderate precocious puberty and explores whether this combined approach offers benefits beyond traditional herbal medicine alone. Participants will be randomly assigned to one of two groups. One group will receive Ziyin-Xiehuo traditional Chinese medicine granules twice daily along with intradermal acupuncture point stimulation targeting specific points, applied three times daily with needles changed every two days, for a duration of six months. The other group will receive only the traditional Chinese medicine granules twice daily for the same six-month period. This design allows comparison between combined therapy and herbal medicine alone. During the study, researchers will monitor participants' breast development changes, particularly the reduction or disappearance of mammary nucleus size at three months. They will also assess bone age changes compared to chronological age over six months. Various evaluations such as ultrasound measurements of uterus and ovary size, Tanner staging, and hormone treatment history will be collected. Safety and efficacy will be carefully observed throughout the six-month treatment period.

CONDITIONS

Brief Title

A Trial of Chinese Traditional Medicine Combining With Intradermal Acupuncture for Treating Precocious Puberty

Who Can Participate

Age: 4Years - 9Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Girls diagnosed with idiopathic precocious puberty with onset age less than or equal to 7.5 years
  • Breast development at Tanner stage III or below, mammillary nucleus diameter 3 cm or less
  • Ultrasound showing uterus volume at least 3 ml, ovary volume at least 1.5 ml, follicle diameter 4 mm or less
  • Bone age less than 1 year older than chronological age and less than 10 years old
  • No prior treatment with GnRH analogs or sex hormones
  • All above criteria must be met simultaneously
Not Eligible

You will not qualify if you...

  • Precocious puberty caused by central nervous system organic diseases
  • Precocious puberty caused by congenital hypothyroidism, congenital adrenal hyperplasia, adrenal tumor, ovarian or testicular tumors, or McCune-Albright syndrome
  • Precocious puberty with family history of tumor, leukemia, diabetes, or systemic lupus erythematous
  • Pseudo sexual precocity or partial precocious puberty

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 months

Participants receive traditional Chinese medicine with or without intradermal acupuncture for idiopathic precocious puberty.

Regular visits for treatment monitoring and assessments during the 6-month period

Trial Site Locations

Total: 2 locations

1

Children's Hospital of Fudan university

Shanghai, Shanghai Municipality, China, 201102

Actively Recruiting

2

Children's Hospital of Fudan University

Shanghai, China, 201102

Actively Recruiting

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Research Team

H

Han Xinghui, Master

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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