Genotype and Phenotype Registry: Enrollment of Normal Control Subjects for Current and Future Research
Registry program for volunteers who are willing to serve as control subjects in future research studies.
|Study Design:||Observational Model: Cohort
Time Perspective: Prospective
|Official Title:||TAP0307: Enrollment of Normal Control Subjects for Current and Future Research|
Cheek cell DNA sample will be collected
|Study Start Date:||February 2004|
|Study Completion Date:||August 2012|
|Primary Completion Date:||August 2012 (Final data collection date for primary outcome measure)|
The registry is a collection of volunteers willing to participate as control subjects in research studies. Control subjects are people who do not have a specific disease; therefore they can serve a critical role as a comparison with people who have the disease or other characteristic being studied. Once registered, participants will be notified about studies they may be able to participate in as a control.
- signing a consent form
- answering a short health survey
- providing a DNA sample via a mouthwash kit
The registry allows scientists to select study participants based on whether or not they have a specific genetic change that may be relevant to a disease under investigation. Having the ability to access controls when needed is an extremely valuable resource that will speed up scientific discoveries.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00926042
|United States, New York|
|The Feinstein Institute for Medical Research|
|Manhasset, New York, United States, 11030|
|Principal Investigator:||Peter K Gregersen, MD||North Shore Long Island Jewish Health System|