% Resolution of incontinence (<1 episode/24 hrs) | W2 | W8 | W12 | W12|W8 | W12|~W8 | |
---|---|---|---|---|---|---|
Placebo | 20,99% | 34,66% | 27,84% | 80,33% | 14,16% | |
Fesoterodine 4 mg | 30,41% | 50,00% | 43,67% | 87,34% | 21,05% | |
Fesoterodine 8 mg | 40,59%a | 55,38%a | 50,21% | 90,65% | 24,20% | |
Tolterodine | 29,23% | 49,47% | 38,18% | 77,17% | 13,04% | |
Solifenacin 5 mgc | 31,49% | 51,99% | 41,76% | 80,33%d | 21,24% | |
Solifenacin 10 mge | 32,11%a | 53,01%a | 42,58% | 80,33%d | 21,66%b | |
Other data | % Nocturia (> = 2 episodes/night) % of patients with nocturia at baseline without nocturia at W12 | Constipation | ||||
Placebo | 54,34% | 1,99% | ||||
Fesoterodine 4 mg | 55,56% | 4,15% | ||||
Fesoterodine 8 mg | 55,90% | 6,01% | ||||
Tolterodine | 57,69% | 2,76% | ||||
Solifenacin 5 mg | 54,34%i | 3,53%j | ||||
Solifenacin 10 mg | 88,72%j | 7,72%j | ||||
Discontinuation | W2 | W8 | W12 | W24 f | W52 f | |
Placebo | 100% | 92,84% | 90,64% | 79,32% | 59,27% | |
Fesoterodine 4 mg | 100% | 92,67%g | equal to placebo data h | |||
Fesoterodine 8 mg | -- | -- | equal to placebo data h | |||
Tolterodine | 100% | 95,76% | equal to placebo data h | |||
Solifenacin 5 mg | 100% | 94,06% | equal to placebo data h | |||
Solifenacin 10 mg | -- | -- | equal to placebo data h |