A Multicenter, Longitudinal, Observational Study in Children With Achondroplasia
Status: Recruiting
Location: See all (8) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY
The goal of this observational study is to collect the anthropometric parameters, clinical characteristics, related medical complications, health-related quality of life and treatments of children with ACH, and complete a natural history observation of ACH for at least 6 months and up to 2 years.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 2
Maximum Age: 11
Healthy Volunteers: f
View:
• Prior to screening, the guardians and children with ACH (if applicable) must be willing and able to provide signed informed consent.
• Clinical diagnosis of ACH confirmed FGFR3 mutation by genetic testing.
• Male or female aged ≥2.5 to \<11 years old at screening.
• Tanner Stage 1 breast development for females or Tanner Stage 1 external genitalia development for males at screening.
• Ambulatory and able to stand without assistance.
Locations
Other Locations
China
Beijing Children's Hospital, Capital Medical University
RECRUITING
Beijing
Chengdu Women's and Children's Central Hospital
NOT_YET_RECRUITING
Chengdu
West China Second University Hospital, Sichuan University
ACTIVE_NOT_RECRUITING
Chengdu
Guangzhou Women and Childrens Medical Center
NOT_YET_RECRUITING
Guangzhou
Children's Hospital Zhejiang University School of Medicine
NOT_YET_RECRUITING
Hangzhou
Xin Hua Hospital Affiliatod to Shanghai Jiao Tong University School of Medicine
RECRUITING
Shanghai
Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology