Rosalind Franklin Society Proudly Announces the 2023 Award Recipient for Psychedelic Medicine
Psychedelic Medicine September 1, 2024 DOI: 10.1089/psymed.2024.65789.rfs2023 via OpenAlex
Summary
AI-generated from the abstractHigh-dose dextromethorphan (DXM) and psilocybin both increased ratings of personal meaning, spiritual significance, psychological challenge, and psychological insight compared to placebo, and these experiences predicted psychological benefit one week later, even when expectancy effects were minimized. The effects tended to favor psilocybin in a dose-dependent manner, and DXM's utility was limited by poor physical tolerability. The findings suggest that dissociatives administered in supportive, psychedelic-like contexts may have therapeutic potential.
Study at a glance
| Characteristics | Randomized controlled trial Double-blind Peer reviewed |
|---|---|
| Sample size | 20 |
| Population | Healthy participants with histories of hallucinogen use |
| Interventions | Dextromethorphan Psilocybin |
| Dose | 400 mg/70 kg DXM, 10, 20, 30 mg/70 kg psilocybin |
| Duration | Single acute dose, assessments at 7 hours and 1 week after each administration |
| Keywords | Art history |
| Registration | NCT02033707 |
| Key finding | High-dose DXM and psilocybin produced similar increases over placebo in ratings of drug experience that predicted psychological benefit at 1 week, with effects favoring psilocybin in a dose-dependent manner. |
Abstract
Rationale: N-methyl-D-aspartate receptor-mediated dissociatives and serotonergic hallucinogens are being increasingly used in therapeutic interventions that involve nonordinary states of consciousness and may represent a unique mental health paradigm wherein pharmacologically induced experiences are conducive to psychological well-being. Objective: The aim of this study was to further understand how the phenomenological and health-promoting effects of high-dose dextromethorphan (DXM) compared to psilocybin in the same participants when administered under experimental conditions that are typical of therapeutic psychedelic trials. Methods: Single, acute oral doses of DXM (400 mg/70 kg), psilocybin (10, 20, 30 mg/70 kg), and inactive placebo were administered under double-blind and psychologically supportive conditions to 20 healthy participants with histories of hallucinogen use. Ratings of personal meaning, spiritual significance, psychological challenge, and psychological insight attributed to acute drug experiences were assessed 7 h (at session end) and 1 week after each drug administration. Persisting psychological effects were assessed 1 week after each drug administration. Results: High-dose DXM and psilocybin produced similar increases over placebo in ratings of drug experience that was predictive of psychological benefit at 1 week, even when expectancy effects were minimized. These effects tended to favor psilocybin in a dose-dependent manner and were limited by poor physical tolerability for DXM. Conclusions: This analysis suggests the utility of exploring clinical applications of dissociatives that occur within the supportive contexts that are characteristic of psychedelic research and that prioritize the optimization of psychologically valuable drug experiences. This study was registered with ClinicalTrials.gov (NCT02033707).