73.1 Participants assessment of success by analysing scores and scales |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
73.1.1 4 weeks |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
73.1.2 16 weeks |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
73.1.3 24 weeks |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
73.2 Any major adverse events (eyelid ptosis, eyelid sensory disorder, strabismus) |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
73.3 Physician assessment of success by analysing scores and scales |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
73.3.1 4 weeks |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
73.3.2 8 weeks |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
73.3.3 12 weeks |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
73.3.4 16 weeks |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
73.3.5 20 weeks |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
73.3.6 24 weeks |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
73.4 Total adverse events |
1 |
|
Risk Ratio (IV, Random, 95% CI) |
Totals not selected |
73.5 Duration of treatment |
1 |
|
Mean Difference (IV, Random, 95% CI) |
Totals not selected |