VA Genetic Tissue Banking
NCT00032578 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1000
Last updated 2009-01-21
Summary
This project is a program-wide genetic tissue databank for the Department of Veterans Affairs Cooperative Studies Program (CSP). The genetic tissue bank has four components: a central repository for DNA and other genetic tissue specimens; a Scientific Advisory Committee of individuals with expertise in the genetics and epidemiology of diseases with special importance to the VA (including cardiovascular, neurologic, respiratory, psychological and other disorders); an Ethics Oversight Committee of individuals with expertise in bioethics and the law, as they apply to the collection and use of genetic tissue, and a Coordinating Center that administers the tissue bank, coordinates the scientific and ethics oversight committees, maintains central access to clinical study data linked to the tissue bank, and provides statistical analysis.
Conditions
- Tissue Banking
Sponsors & Collaborators
-
US Department of Veterans Affairs
lead FED
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2000-01-31
Countries
- United States
Study Locations
More Related Trials
-
UW Undiagnosed Genetic Diseases Program
NCT04586075 ·Status: RECRUITING
-
Patient and Provider Confidence and Satisfaction With the Clinical Use of CYP Genetic Variability
NCT02568618 ·Status: TERMINATED ·Phase: EARLY_PHASE1
-
BioGene Bank Cohort Study for Approved Research Requests
NCT02550171 ·Status: COMPLETED
-
Genomics of Fibrin Clot Structure in Patients With Constitutional Dysfibrinogenemia
NCT05233384 ·Status: ACTIVE_NOT_RECRUITING
-
Observational Study of Advanced Data Analytics in Genetic Conditions
NCT05657405 ·Status: RECRUITING
-
Psychiatric Genotype/Phenotype Project Repository
NCT00762866 ·Status: ENROLLING_BY_INVITATION
-
Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network
NCT02450851 ·Status: RECRUITING
-
Finding Genes for Rare Diseases
NCT02724995 ·Status: WITHDRAWN
-
Whole Genome Trio Sequencing as a Standard Routine Test in Patients With Rare Diseases - "GENOME FIRST APPROACH"
NCT03954652 ·Status: COMPLETED ·Phase: NA
-
The 1200 Patients Project: Studying the Implementation of Clinical Pharmacogenomic Testing
NCT01280825 ·Status: RECRUITING
-
Clinical Integration of Genetic Risk Assessment in Family Medicine
NCT00339794 ·Status: COMPLETED
-
Genomic Services Research Program
NCT02595957 ·Status: RECRUITING
-
Interest of High-throughput Sequencing of RNAs for the Diagnosis of Heterogeneous Genetic Diseases
NCT03971292 ·Status: UNKNOWN
-
Neurogenetics Patient Registry
NCT02995538 ·Status: RECRUITING
-
The VetSeq Study: a Pilot Study of Genome Sequencing in Veteran Care
NCT03380819 ·Status: COMPLETED ·Phase: NA
-
Alzheimer's Disease Genetics Study
NCT00064870 ·Status: RECRUITING
-
Blood Specimen Collection For Laboratory Assay Research
NCT06046651 ·Status: RECRUITING
-
FaceBase Biorepository
NCT01252264 ·Status: COMPLETED
-
Polycythemia Vera, Myelofibrosis and Essential Thrombocythemia: Identification of PV, MF & ET Genes
NCT00715247 ·Status: COMPLETED
-
Identification of the Genetic Causes of Rare Diseases With Negative Exome Findings
NCT04315727 ·Status: RECRUITING ·Phase: NA
-
Rare Genetic Disorders of the Breathing Airways
NCT00323167 ·Status: COMPLETED
-
Diagnostic Research in Patients With Rare Diseases -Solving the Unsolved Rare Diseases
NCT04024774 ·Status: RECRUITING
-
Characterization and Contribution of Genome-wide DNA Methylation (DNA Methylation Episignatures) in Rare Diseases With Prenatal Onset
NCT06475651 ·Status: RECRUITING
-
Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing
NCT02558478 ·Status: UNKNOWN
-
Genetic and Epigenetic Basis of Chronic Wounds
NCT03793062 ·Status: RECRUITING