Methods | Randomised, double blind, placebo control, single oral dose. Study duration 4 h Baseline PI = moderate and severe Self assessment at t = 0.30, 1, and then hourly up to 4 h. |
|
Participants | Mainly orthopaedic surgery N = 86 M 49, F 37 Mean age: 32 years |
|
Interventions | Dipyrone 1 g, n = 30 Acetaminophen 1 g, n = 30 Placebo group, n = 30 |
|
Outcomes | PI: standard 4 point scale (0‐3) PR: standard 5 point (0‐4) PGE: nonstandard 4 point scale |
|
Notes | Oxford Quality Score: R1, DB1, W0. Total = 2 | |
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 |