Finnish Genetic Study for Arrhythmic Events
NCT02075866 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 8000
Last updated 2014-03-04
Summary
Finnish Genetic Study for Arrhythmic Events (FinGesture is a prospective case-control study assessing the characteristics and genetic background of consecutive series of autopsy verified out-of-hospital victims of SCD vs. survivors of an acute coronary event in a specific geographical area in northern Finland.
Conditions
- Sudden Cardiac Death
- Acute Coronary Event
Sponsors & Collaborators
-
University of Oulu
lead OTHER
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 1998-01-31
- Primary Completion
- 2017-12-31
- Completion
- 2017-12-31
Countries
- Finland
Study Locations
More Related Trials
-
Genetic Variation in Platelet Aggregation
NCT01576536 ·Status: COMPLETED
-
Genetic Study of Lupus Patients and Their Families
NCT00235378 ·Status: COMPLETED
-
Prospective Multicenter Study on the Identification of Genetic Abnormalities Predisposing to Vasospasm From a Privileged Model: the Primary Raynaud's Phenomenon
NCT02202291 ·Status: COMPLETED ·Phase: NA
-
Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing
NCT02558478 ·Status: UNKNOWN
-
Genetic Architecture of Acute Aortic Syndromes and Aortic Aneurysm.
NCT06353607 ·Status: RECRUITING
-
Genetic and Blood Biomarkers in Neurological and Neuromuscular Diseases
NCT02780531 ·Status: COMPLETED
-
Dent Disease Mutation Genotyping
NCT01783795 ·Status: COMPLETED ·Phase: NA
-
Screening for Genes in Patients With Congenital Neutropenia
NCT02866162 ·Status: COMPLETED
-
Study of Inherited Neurological Disorders
NCT00004568 ·Status: RECRUITING
-
Genes and Phenotype (GAP) A National Resource for Genotype-Phenotype Studies of Immunological and Inflammatory Pathways
NCT01161056 ·Status: COMPLETED
-
Familial Mediterranean Fever and Related Disorders: Genetics and Disease Characteristics
NCT00001373 ·Status: RECRUITING
-
Genetic Study of Patients With Primary Ciliary Dyskinesia
NCT00005650 ·Status: COMPLETED
-
Fangshan / Family-based Ischemic Stroke Study In China
NCT00534742 ·Status: UNKNOWN
-
Clinical Presentation of Genetic Disorders in Patients Attending Genetic Outpatient Clinic of Assiut University Children Hospital
NCT05888155 ·Status: UNKNOWN
-
Genetic Profile In Patients With Ruptured and Unruptured Intracranial Aneurysms
NCT07233915 ·Status: RECRUITING
-
A Genetic Study for Alzheimer Dementia: Case-control Study
NCT06330155 ·Status: NOT_YET_RECRUITING
-
Genetic Variants in Nicotinamide Adenine Dinucleotide (NAD) Synthesis Pathway
NCT03799705 ·Status: COMPLETED
-
Genetic Studies in Familial Dementia
NCT04680013 ·Status: COMPLETED
-
Identification and Characterization of Novel Non-Coding Variants That Contribute to Genetic Disorders
NCT04399694 ·Status: COMPLETED
-
Omics Gaucher Study: Multiomic Approach
NCT05526664 ·Status: ACTIVE_NOT_RECRUITING
-
Genetic Study of Amyotrophic Lateral Sclerosis in Norway
NCT05119387 ·Status: RECRUITING
-
Study of a Candidate Gene Involved in Goldenhar Syndrome.
NCT04056858 ·Status: COMPLETED
-
Functional Genomics of Rare Genetic Diseases: Realization of Innovative Tools With High Diagnostic Power
NCT04152876 ·Status: UNKNOWN
-
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants
NCT05589714 ·Status: RECRUITING
-
Implementation of Molecular Diagnostic Pathways
NCT03084224 ·Status: RECRUITING