tuneTypical Dose
1200–2400 mg per day in 2–3 divided doses
Racetam
4-Hydroxy-2-oxo-1-pyrrolidineacetamide
tuneTypical Dose
1200–2400 mg per day in 2–3 divided doses
watchEffect Window
Acute (1–3 hours) for focus. Weeks for neuroprotective/memory baselines.
check_circleCompliance
WADA NOT PROHIBITED
Overview
Oxiracetam is a racetam-class compound investigated for cognitive impairment and post-stroke deficits. It is used for memory and attention goals, but modern high-quality trial evidence is limited.
Limited studies suggest possible improvements in memory and attention in dementia or post-stroke cognitive deficits. Proposed mechanisms include cholinergic and glutamatergic modulation, but evidence quality varies and many trials are older. Minority claims include learning enhancement in healthy users, which lacks robust support. Net benefit remains uncertain without contemporary well-powered randomized trials.
Positively modulates AMPA and NMDA receptors, enhances acetylcholine and glutamate release, and increases high-affinity choline uptake (HACU) and neuronal ATP production.
Outcomes
Safety
Evidence
Baumel B, et al. "Oxiracetam in the treatment of multi-infarct dementia." Clin Neuropharmacol. 1989.
Population: Patients with multi-infarct dementia
Key findings: Oxiracetam (800 mg twice daily) resulted in statistically significant improvements in memory and global clinical impression compared to placebo.
Oxiracetam (800 mg twice daily) resulted in statistically significant improvements in memory and global clinical impression compared to placebo.
Lim JS, Rha JH, Park JH, et al. Oxiracetam and physical activity in preventing cognitive decline after stroke: A multicenter, randomized controlled trial. Eur Stroke J. 2026;11(1):23969873251350141. doi:10.1093/esj/23969873251350141. PMID:41614470.
Population: High-risk post-stroke patients at risk for cognitive decline.
Dose protocol: Oxiracetam vs placebo for 36 weeks in 457 post-stroke patients
Key findings: No significant difference from placebo on MMSE (P=0.49) or CDR-SB (P=0.38). No drug-exercise interaction found.
Notes: Large well-powered negative trial. Supported regulatory suspension in South Korea.
This large multicenter double-blind randomized trial tested oxiracetam versus placebo over 36 weeks in 457 post-stroke patients at high risk for cognitive decline. Neither MMSE nor CDR-SB scores showed significant differences between groups. There was no interaction between drug and physical activity. The authors concluded that oxiracetam did not demonstrate benefit in preventing post-stroke cognitive impairment, and noted that these findings supported the regulatory decision to suspend its use in South Korea.