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Extended-Release Trospium Chloride Improves Quality of Life in Overactive Bladder
Authors:Roger R. Dmochowski  Matt T. Rosenberg  Norm R. Zinner  David R. Staskin  Peter K. Sand
Affiliation:1. Vanderbilt University School of Medicine, Nashville, TN, USA;2. Mid-Michigan Health Centers, Jackson, MI, USA;3. Western Clinical Research, Torrance, CA, USA;4. Division of Urology, Caritas-St Elizabeth''s Medical Center, Tufts University School of Medicine, Boston, MA, USA;5. Division of Urogynecology and Reconstructive Surgery, NorthShore University HealthSystem, University of Chicago, Pritzker School of Medicine, Evanston, IL, USA
Abstract:ObjectivesOveractive bladder syndrome (OAB) is a urinary condition that often exerts detrimental effects on an individual's quality of life (QoL). A once-daily, extended-release (ER) formulation of the quaternary amine trospium chloride has recently been developed for the treatment of OAB. The pooled health-related QoL (HRQoL) data from two multicenter, parallel-group, double-blind Phase III studies with trospium chloride ER 60 mg were analyzed.MethodsSubjects aged ≥18 years with urinary urgency, frequency, and an average of ≥1 urge urinary incontinence episode per day on a 3-day bladder diary were randomized (1:1) to receive once-daily trospium 60 mg ER or placebo for 12 weeks. HRQoL was assessed at baseline and at Week 12 using the King's Health Questionnaire (KHQ) and the OAB questionnaire (OAB-q).ResultsOverall, 1165 subjects were randomized (trospium ER, n = 578; placebo, n = 587). Trospium ER produced significantly greater improvements from baseline than placebo in seven of the nine KHQ domains. At Week 12, the improvement in mean OAB-q HRQoL total score (from approximately 52 at baseline) was significantly greater with trospium ER than with placebo (+25.8 vs. +20.7; P = 0.0003). Improvements from baseline were seen with trospium ER on all eight of the OAB-q symptom bother scales.ConclusionsOnce-daily trospium 60 mg ER improved the QoL of subjects with OAB, as assessed using the KHQ and the OAB-q, in two large Phase III clinical trials.
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