Efficacy and safety of two doses of tolterodine versus placebo in patients with detrusor overactivity and symptoms of frequency, urge incontinence, and urgency: Urodynamic evaluation

被引:116
作者
Jonas, U
Hofner, K
Madersbacher, H
Holmdahl, TH
Bucher, A
Frick, J
Heidler, H
Pfluger, H
Primus, G
Schmidbauer, C
Zechner, O
Alloussi, S
Anthuber, C
Blau, U
Dimpfl, T
Flach, K
Frohlich, G
Frohneberg, D
Geier, G
Hannappel, J
Hartung, R
Haubensak, K
Herrlinger, A
Hiller, O
Hofstetter, A
Horsch, R
Junemann, KP
Kindt, J
Koszegi, F
Lahm, AW
Lammle, G
Laval, KU
Melchior, H
Methfessel, HD
Rudolph, R
Terhorst, B
Vilmar, W
Weidenfeld, M
Frykman, H
Granberg, G
Haendler, L
Larsson, C
机构
[1] UNIV INNSBRUCK HOSP,A-6020 INNSBRUCK,AUSTRIA
[2] LANSSJUKHUSET KVINNOKLINIKEN,KALMAR,SWEDEN
关键词
D O I
10.1007/BF02201987
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Tolterodine is a new competitive muscarinic receptor antagonist developed for the treatment of the unstable bladder, A total of 242 patients were enrolled in a multicenter, multinational, randomized, double-blind, placebo-controlled study conducted over a period of 4 weeks in patients with detrusor overactivity and symptoms of frequency, urgency, and urge incontinence. The objective of the study was to compare the efficacy and safety of tolterodine given at 1 or 2 mg b.i.d. versus placebo, At week 4 a statistically significant increase in the volume at first contraction (p = 0.030) and maximal cystometric capacity (p = 0.034) was only in the tolterodine 2 mg b.i.d. group. Tolterodine was safe and generally well tolerated. The incidence of dry mouth, as se the most commonly reported adverse event, was only 9% and of mild to moderate intensity.
引用
收藏
页码:144 / 151
页数:8
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