BCAAs in Concussion 3.0
Akiva Cohen · NCT07670195
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 11–23 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 2
- Target enrollment
- 150
- US sites recruiting
- 1
- Study start
- August 5, 2026
- Record last updated
- September 3, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This study is a randomized, placebo-controlled, double-blinded, therapeutic exploratory clinical trial of branched chain amino acids (BCAAs) in the treatment of concussion. The aim of the study is to determine whether administration of high-dose BCAAs compared to placebo promotes concussion recovery.
Being studied: BCAA; Placebo
Conditions: Concussion (Diagnosis); MTBI - Mild Traumatic Brain Injury; Concussion, Brain; Concussion
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Males and females,11 - 23 years of age.
- Weigh at least 40kg.
- Meeting concussion criteria for the American Congress of Rehabilitative Medicine.
a. One or more clinical signs or two or more acute symptoms with at least one VVE abnormality.
- Present within 4 days of injury.
- Post-menarchal females must have a negative urine pregnancy test.
- Informed consent by the participant, or for participants \<18 years old both informed consent by a parent/guardian and child assent.
Exclusion Criteria
- Evidence of moderate or severe TBI, including GCS \<13, TBI requiring hospital admission, or TBI requiring neurosurgical intervention.
- Prior concussion or TBI within 90 days.
- Known history of maple syrup urine disease or known family history of maple syrup urine disease.
- Any investigational drug use within 30 days prior to enrollment.
- Participants who are pregnant, planning on becoming pregnant during the study duration, or breastfeeding.
- Non-English speaking participants or parent/guardian.
Recruiting US locations
Children's Hospital of Philadelphia
Havertown, PA 19083
Site contact: Daniel Corwin, MD · 215-327-2306 · corwind@chop.edu
Study contacts (from the official record)
- Olivia E. Podolak · 8626687645 · podolako@chop.edu
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