Clinical Trials Directory

Trials / Completed

CompletedNCT02920515

Study of Comprehensive Diagnosis and Treatment for Children Precocious Puberty

Multi-site Study of Comprehensive Treatment for Children Precocious Puberty

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
740 (actual)
Sponsor
Ruijin Hospital · Academic / Other
Sex
Female
Age
2 Years – 14 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGTriptorlin or LeuprorelinGonadotrophin releasing hormone agonists (GnRHa)
DRUGZhibo dihuang pillsTraditional Chinese Medicine
DRUGDabu ying pillsTraditional Chinese Medicine

Timeline

Start date
2012-09-01
Primary completion
2015-08-01
Completion
2015-08-01
First posted
2016-09-30
Last updated
2016-09-30

Source: ClinicalTrials.gov record NCT02920515. Inclusion in this directory is not an endorsement.