GWAS Identified Susceptibility Loci for Glucocorticoid-induced FHN in the Chinese Population
NCT02365077 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 2500
Last updated 2021-03-11
Summary
This is a observation clinical trial. We are collecting the patients with glucocorticoid. They were divided into the experiment group (with femur head necrosis) and control group (without femur head necrosis).Then, we will analyse the patients' genome with genome-wide association study (GWAS). Our purpose is to find susceptibility loci for glucocorticoid-induced femur head necrosis in the Chinese population.
Conditions
- Femur Head Necrosis
- Adverse Effect of Glucocorticoids and Synthetic Analogues
Sponsors & Collaborators
-
Xijing Hospital
lead OTHER
Eligibility
- Min Age
- 18 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-01-01
- Primary Completion
- 2023-12-31
- Completion
- 2023-12-31
Countries
- China
Study Locations
More Related Trials
-
Study of Clinical and Molecular Manifestations of Genetic Disorders
NCT00001466 ·Status: COMPLETED
-
Genomics of Fibrin Clot Structure in Patients With Constitutional Dysfibrinogenemia
NCT05233384 ·Status: ACTIVE_NOT_RECRUITING
-
Genetic Study of Insulin-Like Growth Factor-I Receptor Mutations in Patients With Intrauterine Growth Retardation
NCT00005105 ·Status: UNKNOWN
-
Fangshan / Family-based Ischemic Stroke Study In China
NCT00534742 ·Status: UNKNOWN
-
Genetic Data Collection in Adult Participants to Identify Genetic Variants of Known Importance in Non-alcoholic Steatohepatitis (NASH)
NCT05423327 ·Status: TERMINATED ·Phase: NA
-
Verification of Correlation Between Genetic Testing of Nutritional Metabolism and Clinical Biochemical Indicators
NCT03651934 ·Status: UNKNOWN ·Phase: NA
-
Neurogenetics Patient Registry
NCT02995538 ·Status: RECRUITING
-
Next Generation to Identify Genetic Causes of Disease in Patients Participating in NICHD Clinical Protocols
NCT01375543 ·Status: COMPLETED
-
Investigating the Feasibility and Implementation of Whole Genome Sequencing in Patients With Suspected Genetic Disorder
NCT03829176 ·Status: COMPLETED ·Phase: NA
-
Genetic Analysis of Pheochromocytomas, Paragangliomas and Associated Conditions
NCT03160274 ·Status: RECRUITING
-
Copy Number Variation in Prenatal Diagnosis
NCT04561440 ·Status: UNKNOWN
-
Genes Associated With Hereditary and Drug-Induced Gingival Overgrowth
NCT00104026 ·Status: COMPLETED
-
Genetic and Functional Analysis of Craniometaphyseal Dysplasia (CMD)
NCT01630460 ·Status: RECRUITING
-
NCGENES: North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing
NCT01969370 ·Status: COMPLETED ·Phase: NA
-
Genetic Study of Patients and Families With Diaphyseal Medullary Stenosis With Malignant Fibrous Histiocytoma of the Bone
NCT00007046 ·Status: COMPLETED
-
Correlation of Genetic Susceptibility Genes to Inflammatory Bowel Disease in Chinese Han Population
NCT05071742 ·Status: UNKNOWN
-
Next Generation Sequencing Analysis of Patients with Spontaneous Dissection of Cervical Arteries
NCT06862063 ·Status: RECRUITING ·Phase: NA
-
Natural History Study of GEMIN-5 Related Neurodevelopmental Disorder
NCT06776341 ·Status: RECRUITING
-
Gliogene: Brain Tumor Linkage Study
NCT00418899 ·Status: UNKNOWN
-
Study on Susceptibility Genes of Anterior Cruciate Ligament, Patella Dislocation and Discoid Meniscus
NCT04997538 ·Status: RECRUITING
-
Research for Genetic Factors Involved in Congenital Dislocation of Hip: Genome-wide Association Study in Grand West France
NCT02900482 ·Status: COMPLETED
-
Genetic Diagnosis in Congenital Cataracts
NCT05782452 ·Status: COMPLETED
-
Genomic Sequencing in Patients With HCM Undergoing Septal Myectomy
NCT03043209 ·Status: COMPLETED
-
Natural History of Glycosphingolipid Storage Disorders and Glycoprotein Disorders
NCT00029965 ·Status: RECRUITING
-
Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network
NCT02450851 ·Status: RECRUITING