Outcome | Treatment effect (θ) | 95% CI for θ | U-test (p-value) | τ 2 | NNT/NNH (95% CI) |
---|---|---|---|---|---|
Efficacy | |||||
Reduction in 24-hour pain intensity | -1.128 | (-1.364; -0.891) | <0.001 | 0 | - |
Response | 0.856 | (0.628; 1.085) | <0.001 | 0 | 5(3;7) |
PGI | -0.756 | (-1.004; -0.508) | <0.001 | 0 | - |
Tolerability | |||||
Premature study discontinuation due to: | |||||
- Lack of efficacy | -0.962 | (-1.800; -0.124) | (0.024) | 0 | |
- Adverse events | 1.077 | (0.663; 1.490) | <0.001 | 0 | 11 (7; 23) |
- Other | -0.278 | (-0.636; 0.079) | (0.127) | 0 | |
Diarrhoea | 0.233 | (-0.436; 0.903) | (0.307) | 0.307 | |
Dizziness | 0.817 | (0.398; 1.235) | <0.001 | 0 | |
Headache | 0.468 | (0.090; 0.845) | (0.015) | 0 | |
Nausea | 1.306 | (0.942; 1.669) | 0.039 | 0.039 | |
Somnolence | 1.472 | (1.044; 1.900) | <0.001 | 0 |