Genetic Collection Protocol
NCT05272319 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 2230
Last updated 2025-09-10
Summary
This study involves the one-time collection of whole blood or saliva samples for the extraction and storage of DNA for use in ongoing and future ChiLDReN studies.
Conditions
Sponsors & Collaborators
-
Arbor Research Collaborative for Health
lead OTHER
Principal Investigators
-
Ed Doo, MD · National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
-
Katrina Loh, MD · National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
-
John Magee, MD · University of Michigan
-
Lisa Henn, PhD · Arbor Research Collaborative for Health
Eligibility
- Min Age
- 24 Hours
- Max Age
- 25 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-04-06
- Primary Completion
- 2029-05-31
- Completion
- 2029-05-31
Countries
- United States
- Canada
Study Locations
More Related Trials
-
Molecular Genetics of Schizophrenia
NCT00006418 ·Status: COMPLETED
-
Collection and Storage of Human Biospecimens for Research Into Rare Diseases and Medical Conditions
NCT02365376 ·Status: UNKNOWN
-
Genetics of COVID-19 Susceptibility and Manifestations
NCT04371432 ·Status: COMPLETED
-
Genetic Polymorphism and Israeli Top-level Swimmers' Performance and Expertise
NCT01319032 ·Status: UNKNOWN
-
A Study of Genetic Variation Influencing Pain and Response to Opioid Medications
NCT01293994 ·Status: WITHDRAWN
-
Genetic and Metabolic Disease in Children
NCT02650622 ·Status: RECRUITING
-
Study of Clinical and Molecular Manifestations of Genetic Disorders
NCT00001466 ·Status: COMPLETED
-
Observational Study of the Impact of Genetic Testing on Healthcare Decisions and Care in Interventional Pain Management
NCT02485795 ·Status: UNKNOWN
-
Blood Specimen Collection For Laboratory Assay Research
NCT06046651 ·Status: RECRUITING
-
Next Generation to Identify Genetic Causes of Disease in Patients Participating in NICHD Clinical Protocols
NCT01375543 ·Status: COMPLETED
-
Method Comparison and Clinical Specificity Study: Evaluation of the Infinium HD Cytogenetic Abnormality Test
NCT01426308 ·Status: COMPLETED
-
Screening of Healthy Adults for Genetic Variations That Control Fatty Acid Processing
NCT01516125 ·Status: COMPLETED
-
Studies of Children With Metabolic and Other Genetic Disorders
NCT00025870 ·Status: COMPLETED
-
Investigating the Feasibility and Implementation of Whole Genome Sequencing in Patients With Suspected Genetic Disorder
NCT03829176 ·Status: COMPLETED ·Phase: NA
-
Genetic Origin of Lipid Disorders
NCT00277121 ·Status: UNKNOWN
-
Investigation of the Genetics of Hematologic Diseases
NCT02720679 ·Status: RECRUITING
-
Rare and Undiagnosed Disease Research Biorepository
NCT04703179 ·Status: ENROLLING_BY_INVITATION
-
Pharmacogenetic Testing and Chronic Pain
NCT05259865 ·Status: SUSPENDED
-
Dent Disease Mutation Genotyping
NCT01783795 ·Status: COMPLETED ·Phase: NA
-
Genetic Study of Lupus Patients and Their Families
NCT00235378 ·Status: COMPLETED
-
NIEHS Repository of Stored Biological Samples for Future Use
NCT05666739 ·Status: RECRUITING
-
BioGene Bank Cohort Study for Approved Research Requests
NCT02550171 ·Status: COMPLETED
-
Reverse Phenotyping Core
NCT03632239 ·Status: ENROLLING_BY_INVITATION
-
Genetic Studies of Non-Alcoholic Fatty Liver Disease
NCT01629095 ·Status: TERMINATED
-
DNA Sequencing in Clinical Practice, Mayo Clinic Health Tapestry Study
NCT05212428 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA