Racetam
Piracetam
SaveThe original racetam, synthesized in 1964 by UCB Pharma. Modulates AMPA receptors, improves membrane fluidity, and enhances interhemispheric communication. Used clinically in Europe for myoclonus and cognitive impairment.
Quick verdict
The foundational nootropic with the largest racetam evidence base. Benefits are modest and most reliable in elderly or impaired populations. Healthy young adults may notice little.
Evidence score
A rough internal score reflecting quantity, quality, and consistency of human evidence. Not a clinical recommendation.
What the research shows
A Cochrane review of 24 trials in dementia found some evidence of global cognitive improvement but recommended more research. Best-supported use is for cortical myoclonus (high-dose). Mechanism involves AMPA receptor modulation, enhanced membrane fluidity, and improved cerebral microcirculation.
Benefits
- Largest evidence base of any racetam
- Approved for cortical myoclonus in Europe
- May improve cognitive function in age-related decline
- Enhances interhemispheric communication
Dosage notes
Cognitive use: 2400–4800 mg/day in 2–3 divided doses. Myoclonus: up to 20g/day under medical supervision.
Side effects
- Headache (common, often from choline depletion)
- Insomnia
- GI discomfort
- Weight gain (rare)
Who should be cautious
Prescription-only in many European countries. May worsen agitation in dementia with Lewy bodies. Theoretically increases bleeding risk.
What this page cannot tell you
Effect sizes in healthy adults are small to negligible. Works best in populations with some degree of cognitive impairment.
Leaderboard scores
- Memory45
- Focus40
- Mood25
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