Methods | Randomised, double blind, placebo control, single oral dose. Study duration 6 h. Baseline PI = moderate or severe Self assessment at t = 0, 0.5, 1, then hourly up to 6 h. |
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Participants | Dental extraction N = 159 M 84, F 75 Mean age: 27 years |
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Interventions | Dipyrone 500 mg, n = 39 Aspirin 650 mg, n = 31 Flurbiprofen 50 mg, n = 40 Placebo, n = 39 |
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Outcomes | PI: standard 4 point scale (0‐3) PR: 5 point scale (1‐5) standard wording, but nonstandard numbering PGE: standard 5 point scale Adverse events |
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Notes | Oxford Quality Score: R1, DB1, W0. Total = 2 Rescue medication allowed after 1 h |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Not reported |
Allocation concealment (selection bias) | Unclear risk | Not reported |
Blinding (performance bias and detection bias) All outcomes | Unclear risk | Not reported |