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_SUPPLEMENT
    12 weeks of creating monohydrate supplementation at 5 gm, twice per day
  • Microcrystalline Cellulose — OTHER
    Microcrystalline 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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