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Study of Comprehensive Diagnosis and Treatment for Children Precocious Puberty

Central Precocious Puberty Clinical Trial

Official title:
Multi-site Study of Comprehensive Treatment for Children Precocious Puberty

Clinical Trial Summary

This is a prospective, multicentric, comparative, non-randomized interventional study in which subjects diagnosed with central precocious puberty (CPP) and early puberty (EP) were treated for 6 months to compare the effect with GnRHa and traditional Chinese medicines.

Clinical Trial Description

740 girls with CPP and EP participated in this study, all participates were divided into GnRHa group, traditional chinese medicines group and blank group. After at least six months therapy with GnRHa or traditional Chinese medicines, the investigators compare clinical parameters, sex hormone, bone age and ovarian ultrasound in three groups. ;

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02920515
Study type Interventional
Source Ruijin Hospital
Contact
Status Completed
Phase Phase 4
Start date September 2012
Completion date August 2015
View Details
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