Concussion Clinical Trial
Official title:
Vitamin Therapy in Concussion Management: A Randomized Control Trial
NCT number | NCT02382679 |
Other study ID # | 14D.529 |
Secondary ID | |
Status | Terminated |
Phase | N/A |
First received | |
Last updated | |
Start date | March 2015 |
Est. completion date | May 2016 |
Verified date | April 2022 |
Source | Thomas Jefferson University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to assess the efficacy of vitamin therapy in concussion when compared to placebo with respect to multiple endpoints including symptom severity, cognitive performance on computer based neuropsychological testing, post-concussion balance assessment, and post-concussion vestibular-oculomotor function.
Status | Terminated |
Enrollment | 20 |
Est. completion date | May 2016 |
Est. primary completion date | May 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 11 Years to 22 Years |
Eligibility | Inclusion Criteria: - Subjects ages 11-22 - Concussion within 7 days of enrollment - Presenting for treatment at Rothman Institute or Jefferson Concussion Center Exclusion Criteria: - Subjects with recent prior concussion within the past 30 days - Subjects with a history of moderate to severe TBI requiring hospitalization or resulting in prolonged symptoms (>3weeks). - Subjects with known neurologic diagnosis associated with impaired cognitive function other that Attention Deficit Hyperactive Disorder or Attention Deficit Disorder. - Subjects with know allergy to algae, omega-3 fatty acid, or any component of the formulation. - Subjects currently requiring anticoagulants (ie- Warfarin), anti-platelets (ie- Aspirin, Plavix), or any non-steroidal anti-inflammatory drugs (ie- Ibuprofen, Naprosyn). - Subjects with known liver pathology or significantly elevated liver function tests (greater than 3 X normal). - Subjects with a current lower extremity injury that will affect postural stability testing. - Subjects who are pregnant and/or breast feeding. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Thomas Jefferson University | Rothman Institute Orthopaedics |
Bianchi A, Salomone S, Caraci F, Pizza V, Bernardini R, D'Amato CC. Role of magnesium, coenzyme Q10, riboflavin, and vitamin B12 in migraine prophylaxis. Vitam Horm. 2004;69:297-312. Review. — View Citation
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---|---|---|---|---|
Primary | PCSI: Post-Concussion Symptom Inventory | 4 weeks |
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