Biomarkers in Concussion
Not yet recruiting
- Conditions
- Concussion, SevereConcussion, MildConcussion, Intermediate
- Registration Number
- NCT05943561
- Lead Sponsor
- Medstar Health Research Institute
- Brief Summary
This will be an observational study measuring serum Neurofilament Light Chain concentrations and associated symptoms, with a control branch, and a post-concussion branch.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Over 12 years of age Athletes participating on a sports team willing to participate; undergo blood draws either weekly or every two weeks, depending on arm of study.
Exclusion criteria:
Existing active neurodegenerative disorder (ie severe TBI) Active peripheral nerve disorder (ie diabetic neuropathy)
Exclusion Criteria
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Normalization of NfL levels 12 weeks
- Secondary Outcome Measures
Name Time Method Resolution of concussion symptoms 12 weeks