1 Serious adverse events |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
2 Disease‐specific quality of life: number of women with an I‐QOL score improvement ≥ 10 points at 12 months |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
3 Clinician observations: objective measurement of incontinence: change in leak point pressure at 12 months |
1 |
|
Mean Difference (IV, Random, 95% CI) |
Totals not selected |
4 Other adverse event: pain/dysuria: dysuria |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
5 Other adverse event: (new) detrusor overactivity: overactive bladder symptoms |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
6 Other adverse event: de novo urinary retention: urinary retention |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
7 Other adverse event: urinary tract infection |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
8 Other adverse event: haematuria |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |
9 Other adverse event: hesitancy |
1 |
|
Risk Ratio (M‐H, Random, 95% CI) |
Totals not selected |