Relating Genetic and Environmental Risk Scores to Multiple Sclerosis Susceptibility
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|ClinicalTrials.gov Identifier: NCT01617395|
Recruitment Status : Recruiting
First Posted : June 12, 2012
Last Update Posted : August 14, 2019
- Research shows that both genes and the environment influence a person s risk for getting multiple sclerosis (MS). However, it is not possible to accurately predict who will develop MS. Researchers want to study people with MS and their family members. They have developed a Genetic and Environmental Risk Score for MS. This score combines information from a person's medical history and genes. It also includes environmental factors that may be related to developing MS. This study will test this risk score to see if it can help predict who will develop MS.
- To evaluate a score for genetic and environmental risk factors that may help predict whether a person will develop MS.
- Individuals at least 18 years of age who have MS.
- Individuals between 18 to 50 years of age who are the parent, brother, sister, or child of a person with MS.
- People with MS will allow researchers to look at their personal and medical data. These data will have been collected in other MS-related studies.
- Relatives of people with MS will fill out a questionnaire and give blood and saliva samples. They will fill out the questionnaire again one year later.
- Some relatives will have additional optional testing. These tests will include a physical exam and imaging studies. There may also be other tests. These tests may be repeated every 1 to 5 years for 20 years.
|Condition or disease|
Show Detailed Description
|Study Type :||Observational|
|Estimated Enrollment :||2080 participants|
|Official Title:||Integrating Genetic and Environmental Risk Scores Into an Algorithm to Predict Multiple Sclerosis Susceptibility|
|Study Start Date :||May 30, 2012|
Individuals at risk for developing MS
Healthy Volunteer Cohort
Healthy volunteers, ages 18-50, who do not have a known first-degree relative with MS
MS Patients Cohort
MS patients whose first-degree relatives are enrolled in this study
- The primary outcome is diagnosis of MS according to the 2010 revisions to the McDonald criteria. [ Time Frame: 9/24/2040 ]
- Secondary outcome measures include development of MS-like abnormalities on brain imaging studies, abnormalities on laboratory testing, and clinical symptoms and signs. [ Time Frame: 9/24/2040 ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01617395
|Contact: Jenifer E Dwyer||(301) email@example.com|
|Contact: Daniel S Reich, M.D.||(301) firstname.lastname@example.org|
|United States, Maryland|
|National Institutes of Health Clinical Center, 9000 Rockville Pike||Recruiting|
|Bethesda, Maryland, United States, 20892|
|Contact: For more information at the NIH Clinical Center contact Office of Patient Recruitment (OPR) 800-411-1222 ext TTY8664111010 email@example.com|
|Principal Investigator:||Daniel S Reich, M.D.||National Institutes of Health Clinical Center (CC)|