Table 1.
Characteristics of human studies.
| Reference | Population, mean/median age | Sample size, % male | Injury type | Control | NAC(A) dose | Via | First dose | Other doses | Length of follow-up | Outcome(s) measured | Findings |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Amen et al. (34) | Retired NFL players, age: NR | N = 30, 100% | Repeated mild TBI | Self-matched | Diet with NAC | Oral | NR | Diet supplement, dose NR | 2–12 months | Microcognitive test, SPECT image analysis |
|
| Hoffer et al. (35) | Military personnel, median age: 22 years | N = 81, 99% | Mild post blast injury | Placebo | 4 g loading dose | Oral | Up to 72 h | 4 g/day for 4 days followed by 3 g/day for 3 days | 7 days | Hearing loss, headache, confusion, memory, sleep and balance problems, COWA, animal naming |
|
| Clark et al. (36) | Children, mean age: 9 years | N = 14, 60% | Severe, GCS ≤ 8 | Placebo | NAC 140 mg/kg/dose and probenecid 25 mg/kg/dose | NG tube | NR | NAC 70 mg/kg/dose, 17 doses over 3 days and probenecid 10 mg/kg 11 doses over 3 days | 14 days | Adverse events and antioxidant reserve |
|
COWA, controlled oral word association test; GCS, Glasgow coma scale; NAC, N-acetyl cysteine; NR, not reported; SPECT, single-photon emission computed tomography.