Genetic Diagnosis and Human Growth Hormone Treatment in Small for Gestational Age Children With Short Stature
NCT05070234 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 150
Last updated 2021-10-07
Summary
This study is a multi-center, retrospective and non-interventional research. In this study, a total of 150 short children who were small for gestational age and had been treated with recombinant human growth hormone (rhGH) are selected for genetic testing. The aims of this study are to analyze the genetic etiology of SGA children with short stature, and to compare the efficacy and safety of rhGH treatment in subjects with different etiologies.
Conditions
- Small for Gestational Age Infant
- Silver-Russell Syndrome
- Genetic Diseases, Inborn
Interventions
- GENETIC
-
Blood collection for genetic analysis
Genetic tests in this study are sequential testing, including MS-MLPA, whole exome sequencing, whole genome sequencing, as well as RNA-seq.
Sponsors & Collaborators
-
Shanghai Children's Hospital
collaborator OTHER -
Second Affiliated Hospital of Guangzhou Medical University
collaborator OTHER -
Shenzhen Children's Hospital
collaborator OTHER_GOV -
Tongji Hospital
collaborator OTHER -
The Children's Hospital of Zhejiang University School of Medicine
collaborator OTHER -
Chengdu Women's and Children's Central Hospital
collaborator OTHER -
West China Second University Hospital
collaborator OTHER -
The First Affiliated Hospital with Nanjing Medical University
collaborator OTHER -
Changchun GeneScience Pharmaceutical Co., Ltd.
collaborator INDUSTRY -
Chunxiu Gong
lead OTHER
Principal Investigators
-
Chunxiu Gong, doctor · Beijing Children's Hospital
Eligibility
- Min Age
- 2 Years
- Max Age
- 20 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-10-11
- Primary Completion
- 2022-08-30
- Completion
- 2022-08-30
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