this study was an observational study and no interventions were given to the participants
Otherthe participants were recruited and the data as well as blood sample were collected.
NCT Number: NCT04012632
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.
Looking for future studies?
Notify Me7 year–10 year
Female
Observational
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
the participants were recruited and the data as well as blood sample were collected.
Time frame: 3 months
functional SNP loci of the KISS1/GPR54 pathway genes KISS1, KISSIR, PLCB1, PRKCA, and ITPR1 were selected and detected.
Shenzhen Center for Disease Control and Prevention
Other Gov
Polymorphisms in the Kisspeptin/GPR54 Pathway Genes and the Risk of Early Puberty
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT00278915
Bone Diseases, Bone Diseases, Developmental
Birmingham, Alabama, United States
View Trial DetailsNCT00494169
Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Boston, Massachusetts, United States
View Trial DetailsNCT02431416
Endocrine System Diseases, Gonadal Disorders
Örebro, Sweden
View Trial DetailsNCT00094328
Endocrine System Diseases, Familial Testotoxicosis
Birmingham, Alabama, United States
View Trial Details