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. 2018 Jan 15;8:744. doi: 10.3389/fneur.2017.00744

Table 4.

Risk of bias in human trials assessing the role of N-acetylcysteine for traumatic brain injuries.

Selection bias Performance bias Detection bias Attrition bias Reporting bias Other bias


Random sequence generation Allocation concealment
Amen et al. (34)
Ranking High-risk High-risk High-risk Unclear Unclear High-risk High-risk
Explanation Not randomized No allocation concealment No blinding No information provided No information provided Selective results presented Other drugs used, no dosage, compliance not reported

Hoffer et al. (35)
Ranking Low-risk Low-risk Low-risk Low-risk Low-risk Low-risk High-risk
Explanation Randomized Allocation concealment done Blinding of participants and assessors Blinding of outcome assessor All subjects followed to endpoint Trial protocol and study reported Generalizable? (conducted in the military setting)

Clark et al. (36)
Ranking Low-risk Unclear Low-risk Low-risk Low-risk Low-risk High-risk
Explanation Randomized No information provided Blinding of participants and assessors Blinding of outcome assessor All subjects were followed to endpoint Reported prior publication in clinicaltrials.gov Small sample size