Completed

Polymorphisms in the Kisspeptin/GPR54 Pathway Genes and the Risk of Early Puberty

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What is being collected

Data Collection

Collected from past medical records and data - Retrospective
Who is being recruted

Endocrine System Diseases

+ Gonadal Disorders

+ Puberty, Precocious

From 7 to 10 Years
See all eligibility criteria
How is the trial designed

Case-Control

Comparing exposures between individuals with and without disease in order to identify potential risk factors.
Observational
Study Start: September 2016
See protocol details

Summary

Principal SponsorShenzhen Center for Disease Control and Prevention
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: September 1, 2016

Actual date on which the first participant was enrolled.

There was a worldwide early trend in girls'age for puberty onset. The timing of puberty onset varies greatly among individuals, and much of this variation is modulated by genetic factors. This study was designed to explored the association of polymorphisms in KISS1/GPR54 pathway genes and the risk of early puberty in Chinese Han girls.

Official TitlePolymorphisms in the Kisspeptin/GPR54 Pathway Genes and the Risk of Early Puberty
Principal SponsorShenzhen Center for Disease Control and Prevention
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

628 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-Control

These studies compare people who have a disease (cases) with those who don't (controls). The goal is to look back at previous exposures or risk factors to identify what might have contributed to the disease.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Female

Biological sex of participants that are eligible to enroll.

From 7 to 10 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Endocrine System DiseasesGonadal DisordersPuberty, Precocious

Criteria

Inclusion Criteria: \- Clinical diagnosis of central precocious puberty or early and fast puberty. Exclusion Criteria: * The participants who were not the first visit to the hospital and had been treated before. * The participants who were with endocrine disorders.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.
This study has no location dataSave this study to your profile to know when the location data is available.
CompletedNo study centers