Table 3.
Outcome | Group | Baseline | P value | 4 weeks | P value | Change at 4 weeks |
Effect size [95% CI] | 8 weeks | P value | Change at 8 weeks |
Effect size [95% CI] |
---|---|---|---|---|---|---|---|---|---|---|---|
Total pain score | Active | 0.48 ± 0.17 | 0.86 | 0.29 ± 0.12 | <0.001 | −0.18 | −1.061 [−1.574 to −0.541] | 0.22 ± 0.13 | <0.001 | −0.25 | −1.587 [−2.137 to −1.027] |
Placebo | 0.47 ± 0.17 | 0.43 ± 0.13 | −0.04 | 0.43 ± 0.13 | −0.04 | ||||||
Superficial pain | Active | 5.94 ± 2.37 | 0.11 | 4.24 ± 2.15 | <0.001 | −1.70 | −1.059 [−1.571 to −0.539] | 3.21 ± 2.07 | <0.001 | −2.72 | −1.651 [−2.207 to −1.086] |
Placebo | 6.85 ± 2.18 | 6.21 ± 1.52 | −0.63 | 6.24 ± 1.56 | −0.60 | ||||||
Deep pain | Active | 5.79 ± 4.44 | 0.881 | 3.68 ± 3.33 | 0.03 | −2.10 | −0.562 [−1.052 to −0.067] | 2.79 ± 2.86 | 0.0021 | −3.00 | −0.841 [−1.342 to −0.334] |
Placebo | 6.06 ± 4.45 | 5.79 ± 4.13 | −0.27 | 5.55 ± 3.66 | −0.51 | ||||||
Paroxysmal pain | Active | 8.65 ± 4.30 | 0.911 | 4.29 ± 3.05 | <0.001 | −4.36 | −0.991 [−1.500 to −0.476] | 2.79 ± 2.35 | <0.001 | −5.86 | −1.528 [−2.073 to −0.973] |
Placebo | 8.56 ± 4.34 | 7.55 ± 3.51 | −1.02 | 7.22 ± 3.37 | −1.33 | ||||||
Evoked pain | Active | 8.99 ± 6.11 | 0.551 | 7.02 ± 5.28 | 0.25 | −1.97 | −0.283 [−0.768 to 0.203] | 6.27 ± 4.82 | 0.09 | −2.72 | −0.423 [−0.909 to 0.067] |
Placebo | 8.25 ± 5.79 | 8.51 ± 5.19 | 0.25 | 8.39 ± 5.20 | 0.14 | ||||||
Paraesthesia | Active | 8.96 ± 3.02 | 0.201 | 4.77 ± 3.00 | 0.01 | −4.18 | −0.642 [−1.135 to −0.145] | 3.12 ± 2.57 | <0.001 | −5.83 | −1.473 [−2.014 to −0.922] |
Placebo | 7.91 ± 3.47 | 6.77 ± 3.22 | −1.14 | 7.08 ± 2.79 | −0.83 |
Active n = 33, Placebo n = 33. Statistical significance set at P = < 0.05
1 Shapiro–Wilk distribution test found these data (in one or both arms) to be not normally distributed
Tests of significance are performed nonparametrically with Mann–Whitney U scores given as average ± standard deviation