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. 2009 Sep;68(3):322–341. doi: 10.1111/j.1365-2125.2009.03433.x

Table 1.

Schematic overview of studies involving acetysalicylic acid in human experimental pain models

Reference Dose Model (pain assessments) Main findings
Acute models [10] (n= 30) Topical application (0.03–5%) Intradermal continuous infusion of phosphate buffered solution (pH 5.2) VAS Doses > 1.5% VAS↓
[8] (n= 32) 1000 mg p.o. Intracutaneous electrical stimulation VAS, evoked brain potentials VAS ↓, amplitudes of evoked potentials ↓ latencies of evoked potentials ↔
[13] (n= 14) 1000 mg i.v. Stimulation of nasal mucosa by CO2 VAS, evoked brain potentials, power spectrum PDT ↔
Amplitudes and latencies of evoked potentials ↓, power spectrum changed
[9] (n= 9) 750 mg p.o. Laser skin stimulation, evoked brain potentials Amplitude ↓
[14] (n= 24) 600 and 900 mg p.o. Ischaemic pain AUCVAS, PTT No parameters were affected
[12] (n= 10) 1200 mg p.o. Electrical stimulation of dental pulp PDT PDT ↑
Models inducing hyperalgesia [16] (n= 60) 900 mg p.o. Delayed-onset muscle soreness VAS, McGill questionnaire, deep pressure PDT No parameters were affected
[15] (n= 10) Topical application (0.25 g ml−1) Topically applied capsaicin, evoked pain, area of secondary HA to pinprick and heat and allodynia to light touch Area of HA to pinprick and allodynia to light touch↓
Area of HA to heat ↔
[11] (n= 12) 100 and 1500 mg p.o. Long-lasting pinching of the interdigital web (two different intensities) PDT PDT ↑
Only the highest intensity discriminated between doses

In the column ‘Model’ the method for pain assessment is normal font, and the method for pain induction is bold. PDT, pain detection threshold; PTT, pain tolerance threshold; AUC, area under curve; VAS, visual analogue scale; HA, hyperalgesia.