1 Mean change from baseline in pain |
1 |
|
Mean Difference (IV, Random, 95% CI) |
Totals not selected |
1.1 Risedronate vs. etidronate |
1 |
|
Mean Difference (IV, Random, 95% CI) |
0.0 [0.0, 0.0] |
2 Number of participants who experienced adverse events related to use of bisphosphonates |
2 |
212 |
Risk Ratio (M‐H, Random, 95% CI) |
0.98 [0.72, 1.35] |
2.1 Risedronate vs. etidronate |
1 |
123 |
Risk Ratio (M‐H, Random, 95% CI) |
0.98 [0.68, 1.43] |
2.2 Alendronate vs. etidronate |
1 |
89 |
Risk Ratio (M‐H, Random, 95% CI) |
0.98 [0.55, 1.76] |
3 Number of participants who withdrew due to adverse events |
2 |
212 |
Risk Ratio (M‐H, Random, 95% CI) |
0.69 [0.25, 1.89] |
3.1 Risedronate vs. etidronate |
1 |
123 |
Risk Ratio (M‐H, Random, 95% CI) |
0.79 [0.22, 2.79] |
3.2 Alendronate vs. etidronate |
1 |
89 |
Risk Ratio (M‐H, Random, 95% CI) |
0.56 [0.11, 2.90] |
4 Mean percentage change from baseline in serum total alkaline phosphatase level |
2 |
212 |
Mean Difference (IV, Random, 95% CI) |
‐40.95 [‐49.09, ‐32.81] |
4.1 Risedronate vs. etidronate |
1 |
123 |
Mean Difference (IV, Random, 95% CI) |
‐43.9 [‐48.06, ‐39.74] |
4.2 Alendronate vs. etidronate |
1 |
89 |
Mean Difference (IV, Random, 95% CI) |
‐35.1 [‐45.85, ‐24.35] |
5 Number of participants who achieved normalised alkaline phosphatase level |
2 |
212 |
Risk Ratio (M‐H, Random, 95% CI) |
4.30 [2.72, 6.79] |
5.1 Risedronate vs. etidronate |
1 |
123 |
Risk Ratio (M‐H, Random, 95% CI) |
4.81 [2.58, 8.98] |
5.2 Alendronate vs. etidronate |
1 |
89 |
Risk Ratio (M‐H, Random, 95% CI) |
3.78 [1.93, 7.38] |