1 Pain on weight bearing (0‐100 mm VAS) |
1 |
|
Mean Difference (IV, Fixed, 95% CI) |
Subtotals only |
1.1 1 to 4 weeks post‐injection |
1 |
176 |
Mean Difference (IV, Fixed, 95% CI) |
‐1.0 [‐8.41, 6.41] |
1.2 5 to 13 weeks post‐injection |
1 |
176 |
Mean Difference (IV, Fixed, 95% CI) |
1.0 [‐7.83, 9.83] |
1.3 14 to 26 weeks post‐injection |
1 |
176 |
Mean Difference (IV, Fixed, 95% CI) |
5.0 [‐4.98, 14.98] |
2 Lequesne Index (0‐24) |
1 |
|
Mean Difference (IV, Fixed, 95% CI) |
Subtotals only |
2.1 1 to 4 weeks post‐injection |
0 |
0 |
Mean Difference (IV, Fixed, 95% CI) |
0.0 [0.0, 0.0] |
2.2 5 to 13 weeks post‐injection |
0 |
0 |
Mean Difference (IV, Fixed, 95% CI) |
0.0 [0.0, 0.0] |
2.3 14 to 26 weeks post‐injection |
1 |
180 |
Mean Difference (IV, Fixed, 95% CI) |
1.0 [‐0.37, 2.37] |
3 Number of clinical failures |
1 |
|
Risk Ratio (M‐H, Fixed, 95% CI) |
Subtotals only |
3.1 14 to 26 weeks post‐injection |
1 |
176 |
Risk Ratio (M‐H, Fixed, 95% CI) |
0.32 [0.07, 1.54] |
3.2 45 to 52 weeks post‐injection |
1 |
136 |
Risk Ratio (M‐H, Fixed, 95% CI) |
0.86 [0.58, 1.28] |
4 Number of survivors (patients not requiring additional treatment for study knee) (45 to 52 weeks post‐injectio |
1 |
|
Risk Ratio (M‐H, Fixed, 95% CI) |
Subtotals only |
5 Safety: number of patients withdrawn due to adverse events (45 to 52 weeks post‐injection) |
1 |
|
Risk Ratio (M‐H, Fixed, 95% CI) |
Subtotals only |
6 Safety: number of adverse events related to treatment (45 to 52 weeks post‐ injection) |
1 |
|
Risk Ratio (M‐H, Fixed, 95% CI) |
Subtotals only |
7 Safety: number of patients reporting adverse events (45 to 52 weeks post‐ injection) |
1 |
|
Risk Ratio (M‐H, Fixed, 95% CI) |
Subtotals only |