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Fluvoxamine-controlled release formulation for the treatment of generalized social anxiety disorder.

机译:氟伏沙明控释制剂用于治疗广泛性社交焦虑症。

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BACKGROUND: Generalized social anxiety disorder is a highly prevalent anxiety disorder with deleterious effects on social and family relationships, as well as work performance. We report the results of a multicenter, randomized, placebo-controlled trial comparing the efficacy, safety, and tolerability of fluvoxamine controlled release (CR) to placebo in patients with generalized social anxiety disorder. METHODS: A total of 279 adult patients meeting all inclusion/exclusion criteria was recruited at 23 United States sites and randomly assigned to receive either fluvoxamine CR (100-300 mg/d) or placebo for 12 weeks. The dose could be increased, based on efficacy and tolerability, in increments of 50 mg/d at weekly intervals. The dosage remained constant during weeks 6 to 12. RESULTS: Treatment with fluvoxamine CR resulted in statistically and clinically significant improvements in symptoms associated with generalized social anxiety disorder as early as week 4 on the Liebowitz Social Anxiety Scale and theClinical Global Impression Scale Global Improvement, and at week 6 on the Sheehan Disability Scale, Clinical Global Impression Scale Severity of Illness and the Patient Global Impression of Improvement Scale. The most frequent adverse events reported by patients on fluvoxamine CR were headache, nausea, somnolence, and insomnia. No weight gain was observed for either treatment group, and at end point, there were no differences between treatments on overall sexual function, as measured by the Arizona Sexual Experience Scale. CONCLUSIONS: Both physician and patient-rated scales indicate that fluvoxamine CR is effective and safe for the treatment of generalized social anxiety disorder.
机译:背景:广泛性社交焦虑症是一种高度流行的焦虑症,对社会和家庭关系以及工作绩效产生有害影响。我们报告了一项多中心,随机,安慰剂对照试验的结果,该试验比较了氟伏沙明控释(CR)对安慰剂在广义社交焦虑症患者中的疗效,安全性和耐受性。方法:在美国的23个地点招募了满足所有纳入/排除标准的279名成年患者,并随机分配接受氟伏沙明CR(100-300 mg / d)或安慰剂治疗12周。基于功效和耐受性,剂量可以每周间隔增加50 mg / d。剂量在第6到12周内保持恒定。结果:最早在利勃维茨社交焦虑量表和临床总体印象量表的全球改善范围内,氟伏沙明CR治疗最早在第4周就导致了与广泛性社交焦虑症相关的症状的统计学和临床​​显着改善,在第6周时,评估了Sheehan残疾量表,临床总体印象量表,疾病严重度和患者总体印象改善量表。氟伏沙明CR患者报告的最常见不良事件为头痛,恶心,嗜睡和失眠。在两个治疗组中均未观察到体重增加,并且最终,根据亚利桑那性经验量表的测量,治疗之间的总体性功能没有差异。结论:医师和患者评分量表均表明氟伏沙明CR治疗广泛性社交焦虑症有效且安全。

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