64.1 Participant assessment of success by analysing scores and scales |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
64.1.1 4 weeks |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
64.1.2 8 weeks |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
64.1.3 12 weeks |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
64.1.4 16 weeks |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
64.2 Any major adverse events (eyelid ptosis, eyelid sensory disorder, strabismus) |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
64.3 Physician assessment of success by analysing scores and scales |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
64.3.1 4 weeks |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
64.3.2 8 weeks |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
64.3.3 12 weeks |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
64.3.4 16 weeks |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
64.4 Total adverse events |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |