Fangshan / Family-based Ischemic Stroke Study In China
NCT00534742 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1500
Last updated 2011-12-14
Summary
The exact etiology of ischemic stroke remains unclear, because multiple genetic predispositions and environmental risk factors may be involved, and their interactions dictate the complexity. Family-based studies provide unique features in design because of their robustness to population admixture and stratification. The Fangshan / Family-based Ischemic Stroke Study In China (FISSIC) program aims to conduct a genetic pedigree study of ischemic stroke in rural communities of China.
Conditions
Sponsors & Collaborators
-
National Natural Science Foundation of China
collaborator OTHER_GOV -
Ministry of Education, China
collaborator OTHER_GOV -
Ministry of Science and Technology of the People´s Republic of China
collaborator OTHER_GOV -
Peking University
lead OTHER
Principal Investigators
-
Yonghua Hu, MD · Peking University School of Public Health
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-06-30
- Primary Completion
- 2015-12-31
- Completion
- 2015-12-31
Countries
- China
Study Locations
More Related Trials
-
Implementation of Molecular Diagnostic Pathways
NCT03084224 ·Status: RECRUITING
-
Familial Intracranial Aneurysm Study II
NCT00071565 ·Status: COMPLETED
-
Genetic Profile In Patients With Ruptured and Unruptured Intracranial Aneurysms
NCT07233915 ·Status: RECRUITING
-
Genetics of Type 2 Diabetes Among Han Chinese
NCT00837408 ·Status: COMPLETED
-
Prevalence of Genetic Polymporphism on RNF213 rs112735431 Gene in Non-cardioemboli Ischemic Cerebrovascular Disease
NCT02720861 ·Status: UNKNOWN
-
Genetic Analysis of Familial Brain Aneurysms
NCT00011856 ·Status: COMPLETED
-
Cancer Risk Assessment in Patients With a Constitutional Alteration of the PTEN Gene
NCT05630105 ·Status: SUSPENDED
-
Identification of New FTLD Genes
NCT02363062 ·Status: UNKNOWN
-
The Fondazione Genomic SARS-CoV-2 Study COVID-19
NCT06549712 ·Status: COMPLETED ·Phase: NA
-
PROGENI (Parkinson's Research: The Organized Genetics Initiative) Family Study of LRRK2 (Leucine-rich Repeat Kinase 2)
NCT01536821 ·Status: COMPLETED
-
Genetic Analysis of Pheochromocytomas, Paragangliomas and Associated Conditions
NCT03160274 ·Status: RECRUITING
-
Genetic and Blood Biomarkers in Neurological and Neuromuscular Diseases
NCT02780531 ·Status: COMPLETED
-
Clinical and Molecular Studies in Families With Inherited Eye Disease
NCT02771236 ·Status: RECRUITING
-
Genetics of Familial and Sporadic ALS
NCT00821132 ·Status: COMPLETED
-
Genetics in the Progression of Nephropathies
NCT06416761 ·Status: RECRUITING
-
Genetic Analysis of Familial Melanoma
NCT00339404 ·Status: COMPLETED
-
Observational Study of Advanced Data Analytics in Genetic Conditions
NCT05657405 ·Status: RECRUITING
-
Study of the Genome, Gut Metagenome and Diet of Patients With Incident Parkinson's Disease
NCT04119596 ·Status: TERMINATED
-
Establishment of Genetic Basis for Neurological Disease by Genetic Screening
NCT03322306 ·Status: ENROLLING_BY_INVITATION
-
Multi-center Registration Study of Adult Onset Still's Disease in Chinese Population
NCT03651193 ·Status: UNKNOWN
-
Clinical and Genetic Studies of Familial Presenile Dementia With Neuronal Inclusion Bodies
NCT00006176 ·Status: COMPLETED
-
Genetic Factors in Chronic Sinusitis
NCT00880516 ·Status: ACTIVE_NOT_RECRUITING
-
Study of Inherited Neurological Disorders
NCT00004568 ·Status: RECRUITING
-
The Imaging Genetic Study of Schizophrenia and Family
NCT01259232 ·Status: UNKNOWN
-
Genetic Study of Brain Tumors in Young Children
NCT00010101 ·Status: TERMINATED