Found 42 genetics trials
A listing of genetics medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.
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This is a retrospective cohort study which primarily aims to understand if a patients UGT1A1 phenotype affects patients' clinical outcomes following treatment with sacitizumab. Patients will be consented for prospective sample collection to perform genotyping. The genotyping will be performed in a research laboratory and will not be returned to …
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The overarching goal of our research is to define an evidence-based, sustainable approach to identifying and managing genetic risk among young adults with cancer and their relatives. Conventional practice leaves referral and testing decisions to mostly non-expert clinicians implementing complex guidelines at the point of care, leading to substantial under-utilization. …
Dr. Amit Bar-Or, MD, FRCPC from the University of Pennsylvania Department of Neurology is conducting a study to investigate how the structure and activity of gastrointestinal microbes (bacteria and fungi) found in the gut contribute to multiple sclerosis pathogenesis. You are being asked to participate in this study because either …
The purpose of this study is to investigate prostate cancer in individuals who have a genetic risk for the disease. Prostate cancer is a common cancer in men, especially those with inherited genetic changes in certain genes like BRCA1, BRCA2, ATM, TP53, and HOXB13. These genetic changes can increase the …
This study investigates the use of a digital chatbot-enabled intervention compared to standard remote genetic services to increase the uptake of genetic counseling and testing among adolescents and young adult (AYA) cancer patients. Genetic testing helps identify cancer predisposition syndromes, which can guide enhanced screening and preventive measures. However, many …
The objective of this study is to identify families and individuals with tumors and characterize inherited genetic variation. The outcome of the study is the identification of novel high and low penetrance cancer susceptibility alleles. This is expected to significantly advance our knowledge of the development of cancer and has …
The research study is being conducted to better understand factors that lead to gastric (stomach) cancer, including differences in our genes that may put some people at increased risk of developing gastric cancer compared to other people. Both people with increased risk as well as people with average risk of …
PRIMARY OBJECTIVE: To conduct a multicenter, observational study of patients with well-characterized hepatic adenoma. At the end of the study, robust clinical information, central bio-repository of genomic DNA and liver tissue (where available) will be developed SECONDARY OBJECTIVE: To develop the well characterized hepatic adenoma biorepository with linked clinical data …
The goal of the eREACH3 Study is to evaluate the implementation of digital tools into remote genetic services, evaluating uptake and use of digital tools and outcomes in representative clinical populations. Our primary endpoints will include uptake of services and digital alternatives (future amendments). We will use proportions and 95% …
Identification of actionable genetic alterations is critical to determining the appropriate therapy in unresectable non-small cell lung cancer (NSCLC). Red blood cells (RBCs) may be an abundant and long-lasting reservoir of detectable tumor DNA. A "liquid biopsy," using blood samples from patients with advanced NSCLC to identify targetable mutations from …
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