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Summary of Findings From the FDA Regulatory Science Forum on Measuring Sexual Dysfunction in Depression Trials

机译:FDA监管科学论坛关于测量抑郁症试验中的性功能障碍的研究结果摘要

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摘要

Objective: Sexual dysfunction is a significant treatment-emergent adverse reaction to the serotonergic antidepressants (selective serotonin reuptake inhibitors [SSRIs] and serotonin-norepinephrine reuptake inhibitors [SNRIs]). However, the rate of sexual dysfunction is often underestimated in registration trials, which have relied on unsolicited reports. We conducted a literature search to examine the rates of sexual dysfunction with SSRIs/SNRIs when these rates were ascertained by structured questionnaires or standardized instruments. Additionally, we conducted exploratory analyses of major depressive disorder (MDD) registration trial data.
机译:目的:性功能障碍是对5-羟色胺能抗抑郁药(选择性5-羟色胺再摄取抑制剂[SSRIs]和5-羟色胺-去甲肾上腺素再摄取抑制剂[SNRIs])产生的重大治疗不良反应。但是,在注册试验中,性功能障碍的发生率常常被低估了,而注册试验依赖于未经请求的报告。我们进行了文献检索,以检查通过结构化问卷或标准化工具确定SSRI / SNRI引起的性功能障碍的比率。此外,我们对主要抑郁症(MDD)注册试验数据进行了探索性分析。

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