Creatine Supplementation in Pediatric Brain Injury
- Sponsor
- Spaulding Rehabilitation Hospital
- Study ID
- NCT07756060
- Status
- Not Yet Recruiting
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Conditions
- Brain Injury
- Stroke
- Traumatic Brain Injury
Eligibility Criteria
- Sex
- ALL
- Age
- 8 Years - 25 Years
- Healthy Volunteers
- Not accepted
Interventions
- Creatine monohydrate — DIETARY_SUPPLEMENT12 weeks of creating monohydrate supplementation at 5 gm, twice per day
- Microcrystalline Cellulose — OTHERMicrocrystalline cellulose, which is an inert powder that is indistinguishable from creatine monohydrate in all sensory and procedural aspects, including appearance, taste, and solvability
Study Details
A study examining the effects of creatine supplementation to improve recovery after brain injury in children and teenagers.
Key Dates
- First listed
- Aug 10, 2026
- Start date
- Oct 31, 2026
- Status verified
- Aug 2026
- Primary completion
- Jan 31, 2030
- Completion
- Sep 30, 2030
Study Design
- Enrollment
- 46 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Creatine
- Placebo Comparator: Control
Primary Outcome Measure
Recruitment rate [ Time Frame: 12 weeks ]
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