2.1 Participant assessment of success by analysing scores and scales |
4 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Subtotals only |
2.1.1 4 weeks |
4 |
575 |
Risk Ratio (M‐H, Random, 95% CI) |
19.45 [8.60, 43.99] |
2.1.2 8 weeks |
2 |
204 |
Risk Ratio (M‐H, Random, 95% CI) |
28.45 [5.92, 136.74] |
2.1.3 12 weeks |
2 |
203 |
Risk Ratio (M‐H, Random, 95% CI) |
12.77 [2.78, 58.72] |
2.1.4 16 weeks |
2 |
167 |
Risk Ratio (M‐H, Random, 95% CI) |
20.71 [2.82, 151.91] |
2.1.5 24 weeks |
1 |
77 |
Risk Ratio (M‐H, Random, 95% CI) |
4.19 [0.21, 84.41] |
2.2 Major adverse events (eyelid ptosis, eyelid sensory disorder, strabismus) |
8 |
1390 |
Peto Odds Ratio (Peto, Fixed, 95% CI) |
3.62 [1.50, 8.74] |
2.3 Physician assessment of success by analysing scores and scales |
7 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Subtotals only |
2.3.1 4 weeks |
7 |
1339 |
Risk Ratio (M‐H, Random, 95% CI) |
17.10 [10.07, 29.05] |
2.3.2 8 weeks |
6 |
1046 |
Risk Ratio (M‐H, Random, 95% CI) |
21.50 [9.68, 47.75] |
2.3.3 12 weeks |
6 |
1046 |
Risk Ratio (M‐H, Random, 95% CI) |
10.81 [5.79, 20.16] |
2.3.4 16 weeks |
5 |
933 |
Risk Ratio (M‐H, Random, 95% CI) |
15.13 [5.98, 38.27] |
2.3.5 20 weeks |
1 |
77 |
Risk Ratio (M‐H, Random, 95% CI) |
5.86 [0.31, 109.74] |
2.3.6 24 weeks |
1 |
77 |
Risk Ratio (M‐H, Random, 95% CI) |
4.19 [0.21, 84.41] |
2.4 Total adverse events |
8 |
1388 |
Risk Ratio (M‐H, Random, 95% CI) |
1.14 [0.89, 1.45] |
2.5 Duration of treatment (weeks) |
1 |
77 |
Mean Difference (IV, Random, 95% CI) |
18.40 [16.17, 20.63] |