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In older adults, oral THC reduced lab pain, while vaporization raised…

Balancing Analgesic Effects and Abuse Liability in Older Adults: A Randomized, Placebo-Controlled Trial of Oral and Vaporized Δ9-Tetrahydrocannabinol.

medRxiv : the preprint server for health sciences • • Highly Relevant
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AI Summary

This randomized, double-blind, placebo-controlled laboratory trial asked whether oral or vaporized Δ9-THC could reduce pain sensitivity in adults aged 65 and older, and how those effects compared with abuse-related responses. Twenty adults completed three eight-hour sessions, receiving placebo or different doses of oral or vaporized Δ9-THC. The primary pain finding was mixed: oral 5 mg reduced laboratory-evoked pain sensitivity compared with placebo, but the overall dose effect in the oral arm was not significant. Oral 10 mg and both vaporized doses did not differ from placebo on this measure.

Subjective drug effects rose with dose and were strongest after vaporization; reinforcement value increased only after vaporized 4 mg. Oral 5 mg showed pain relief across the reported assessment period, while pleasurable effects peaked later; vaporized Δ9-THC produced pleasurable effects quickly but did not significantly change thermal pain sensitivity. Abuse-related responses tracked Δ9-THC exposure, whereas analgesia did not show a significant association with exposure, and all reported adverse events occurred after vaporized 4 mg. Because this was a small laboratory study using experimentally evoked pain, it cannot establish pain relief or safety in everyday clinical use; this is an abstract-based summary.

💡 Key Findings

1
In this trial of 20 adults aged 65 and older, oral 5 mg Δ9-THC reduced laboratory-evoked pain sensitivity versus placebo, but the oral arm's overall dose effect was not significant; oral 10 mg and both vaporized doses did not differ from placebo.
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2
Subjective drug effects increased with dose and were greatest after vaporization; reinforcement value increased only after vaporized 4 mg.
High
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3
Pain relief after oral 5 mg was observed at assessments from 60 to 360 minutes, while pleasurable effects peaked at 150 minutes. Vaporized Δ9-THC produced pleasurable effects within 30 minutes but did not significantly change thermal pain sensitivity.
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4
Abuse liability tracked Δ9-THC exposure, but analgesia did not show a significant association with exposure; all adverse events occurred at vaporized 4 mg.
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📄 Original Abstract

Cannabis use is rising fastest among older adults in the U.S., and pain is among the most common reasons they use it. No trial, however, has measured the trade-off between the analgesic and abuse-related effects of {Delta}9-tetrahydrocannabinol ({Delta}9-THC) in this population. In a randomized, double-blind, placebo-controlled trial, 20 adults aged 65 and older were assigned to oral {Delta}9-THC (placebo, 5, 10 mg) or vaporized {Delta}9-THC (placebo, 2, 4 mg) across three eight-hour sessions in counterbalanced order. We assessed laboratory-evoked pain sensitivity using quantitative sensory testing, abuse liability using subjective drug effects and reinforcement value, and also sampled plasma {Delta}9-THC and 11-OH-THC. Analgesia and abuse liability outcomes were measured repeatedly within each session. On a pain sensitivity index, oral 5 mg relieved pain relative to placebo (p=.040), although the oral arm's overall dose effect was not significant (p=.108); oral 10 mg and both vaporized doses did not differ from placebo. Subjective effects increased with dose and were greatest after vaporization, whereas reinforcement value increased only after vaporized 4 mg. After oral 5 mg, analgesia exceeded placebo at every assessment (60-360 min), while its pleasurable effects peaked at 150 min. Vaporized {Delta}9-THC produced pleasurable effects within 30 min but did not significantly change thermal pain sensitivity. While abuse liability tracked {Delta}9-THC exposure, analgesia showed no significant association, and all adverse events occurred at vaporized 4 mg. These findings suggest dose and route selection may help maximize {Delta}9-THC analgesia while minimizing abuse liability, a strategy that warrants evaluation in clinical populations.

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