Parkinson's Disease G2019S LRRK2 Genetic Testing Program
NCT04919356 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 836
Last updated 2023-01-18
Summary
Increase awareness of the G2019S LRRK2 mutation in Parkinson's and no cost genetic testing program.
Conditions
Interventions
- GENETIC
-
G2019S LRRK2
No cost genetic testing for G2019S LRRK2
Sponsors & Collaborators
-
Engage Health Inc.
collaborator INDUSTRY -
Sano
collaborator OTHER -
Escape Bio, Inc.
lead INDUSTRY
Principal Investigators
-
Carrolee Barlow, MD, PhD · ESCAPE Bio
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-06-08
- Primary Completion
- 2022-12-05
- Completion
- 2022-12-05
Countries
- United States
Study Locations
More Related Trials
-
Adult Patients With Undiagnosed Conditions and Their Responses to Clinically Uncertain Results From Exome Sequencing
NCT03605004 ·Status: COMPLETED
-
Genetic Analysis of Uncommon Disease Presentations in Non-US Populations
NCT06595940 ·Status: RECRUITING
-
Study to Estimate How Common it is to Have Genetic Variants Associated With NAFLD
NCT04494360 ·Status: COMPLETED
-
Genetic Variation in OCT1 and Response to Metformin
NCT00588172 ·Status: WITHDRAWN ·Phase: PHASE4
-
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease
NCT04620980 ·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
-
A Study to Compare Genetic Variations of IGF-I and IGF-II
NCT01329523 ·Status: COMPLETED
-
Finding Genes for Rare Diseases
NCT02724995 ·Status: WITHDRAWN
-
Observational Study of Advanced Data Analytics in Genetic Conditions
NCT05657405 ·Status: RECRUITING
-
Genetic Studies of Non-Alcoholic Fatty Liver Disease
NCT01629095 ·Status: TERMINATED
-
Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network
NCT02450851 ·Status: RECRUITING
-
Genetic Identification of Monogenic Disorders in Early-onset Stroke Using Targeted Next Generation Sequencing Panel
NCT04485598 ·Status: COMPLETED
-
Genetics of Motor Learning
NCT01105845 ·Status: TERMINATED
-
Research for Individualized Therapeutics in Rare Genetic Disease
NCT05236595 ·Status: ENROLLING_BY_INVITATION
-
Identification of Genomic Loci Determining Susceptibility to the Development of High Myopia
NCT02583620 ·Status: COMPLETED ·Phase: NA
-
Biomarkers in Neurodegenerative Diseases
NCT04055532 ·Status: WITHDRAWN
-
Monogenic Kidney Stone - Genetic Testing
NCT03305835 ·Status: RECRUITING
-
Genetics of COVID-19 Susceptibility and Manifestations
NCT04371432 ·Status: COMPLETED
-
Neurogenetics Patient Registry
NCT02995538 ·Status: RECRUITING
-
A Natural History Study of the Gangliosidoses
NCT00668187 ·Status: RECRUITING
-
Genetic Disease Gene Identification
NCT00916903 ·Status: TERMINATED
-
Next Generation to Identify Genetic Causes of Disease in Patients Participating in NICHD Clinical Protocols
NCT01375543 ·Status: COMPLETED
-
Genetics of Type 2 Diabetes Among Han Chinese
NCT00837408 ·Status: COMPLETED
-
Clinical Integration of Genetic Risk Assessment in Family Medicine
NCT00339794 ·Status: COMPLETED
-
Early Onset Alzheimer's Disease Genomic Study
NCT03645993 ·Status: COMPLETED