Huang · The Journal of clinical psychiatry 2025 · Randomized double-blind placebo-controlled trial · n=77

Efficacy and Safety of Sulforaphane Added to Antipsychotics for the Treatment of Negative Symptoms of Schizophrenia: A Randomized Controlled Trial.

Cited 16 times in the scientific literature.

Level 2 - randomized trial

Individual randomized controlled trial

PubMed 39832347 · doi:10.4088/JCP.24m15272 · record verified 2026-08-30

What was done

A 24-week, double-blind, randomized, placebo-controlled trial evaluated adjunctive high-dose sulforaphane (1,700 mg Avmacol Extra Strength daily, glucoraphanin content 30 mg/tablet) versus placebo in patients with schizophrenia on antipsychotics in Hunan, China. Participants were randomized 2:1 (53 analyzed in the sulforaphane group, 24 in the placebo group who had at least 1 postintervention clinical evaluation). The primary outcome was the change in Positive and Negative Syndrome Scale (PANSS) negative symptoms.

What was found

Sulforaphane-treated patients demonstrated a significantly greater decrease in PANSS negative symptom total score (P = .01) and PANSS negative factor score (P = .02) compared to placebo. The most prominent difference occurred at 24 weeks (P ≤ .001) with a large effect size (d = 0.8). The effect on negative symptoms was not mediated by changes in PANSS depression or cognitive factor scores.

Why it matters

Effective pharmacotherapies for negative symptoms of schizophrenia are limited. This study provides randomized trial evidence that sulforaphane, an HDAC inhibitor with antioxidant properties, may be an effective adjunctive treatment for these persistent symptoms.

Limits

The study had a relatively small sample size (n = 77 analyzed with 2:1 allocation), was conducted in a single geographic region (Hunan, China), and the abstract does not report specific safety/adverse event outcomes, exact baseline or endpoint numerical scores, or long-term post-discontinuation follow-up.

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