Table 2.
Analysis of VAS Pain Intensity Score (intention-to-treat population)
Time point | Adjusteda change from baseline | Estimated treatment effect (95% confidence interval) | p value | |
---|---|---|---|---|
Methoxyflurane (N = 102) | Placebo (N = 101) | |||
Overall | −29.0 | −11.6 | −17.4 (−22.3,−12.5) | <0.0001 |
5 min | −20.7 | −8.0 | −12.6 (−17.0, −8.3) | |
10 min | −27.4 | −11.1 | −16.3 (−21.4,−11.1) | |
15 min | −33.3 | −12.3 | −21.0 (−26.8,−15.3) | |
20 min | −34.8 | −15.2 | −19.7 (−26.0,−13.3) | |
Time by treatment interaction | 0.0004 |
Pain scores recorded following the start of the planned emergency department procedure were excluded from the analysis. Pain scores taken after initiation of rescue medication were included in the analysis
VAS visual analog scale
aLeast squares mean adjusted for baseline VAS pain score and time by treatment interaction