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. 2009 Aug;68(2):149–168. doi: 10.1111/j.1365-2125.2009.03456.x

Table 6.

Schematic overview of studies involving codeine in human experimental pain models

Reference Dose Model Findings
Acute models [99] (n= 18) 125 mg orally Pressure algometry (phalanx), PTT, single and repeated electrical sural nerve stimulation PDT, PTT Cold pressor test peak pain AUCVAS, discomfort Pain and discomfort for all stimulations was decreased
[104] (n= 27) 100 mg orally Heat skin stimulation and deep pressure PDT, PTT Cold pressor test VAS, peak pain, AUCVASSural nerve electrical stimulation, PDT, PTT stimulus response curve Heat from electrical, thermal and pressure ↔, cold pressor, peak pain ↓
[108] (n= 12) 60/120 mg orally Cold pressor test VAS, level of ‘bothersomeness’ VAS ↓ (not dose-related), level of bothersomeness ↔
[107] (n= 14) 75 mg or 100 mg orally Cold pressor test AUCVAS, peak pain, discomfort (VAS) Heat skin stimulation and deep pressure PDT, PTT Peak pain and discomfort in cold pressor test ↓ (only extensive metabolizers) AUCVAS and heat and pressure (PDT and PTT) ↔
[108] (n= 48/32) 60 mg orally Electrical and heat skin stimulation (PDT, PTT (electrical) Pain from both modalities was decreased

In the column ‘model’ the method for pain assessment is normal font, and the method for pain induction is bolded. Abbreviations: pain detection threshold (PDT), pain tolerance threshold (PTT), area under curve (AUC), visual analogue scale score (VAS), hyperalgesia (HA).