NCT03679702Unknown不适用
A Viveve Experience Normalizes Untreated Selective Serotonin Reuptake Inhibitor (SSRI) Sexuality Syndrome
Michael Krychman, MD2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2018年12月15日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 10
- 试验地点
- 2
- 主要终点
- Safety - Adverse Events
研究概览
简要总结
A pilot study to investigate non-surgical treatment for women who suffer from sexual complaints secondary to SSRI Sexuality Syndrome.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Currently using SSRI for 3 months at a stable dose
排除标准
- •Pregnant, currently breastfeeding, or breast-fed within the last 6 months
- •Has any implantable electrical device that could potentially be affected by use of radiofrequency.
研究组 & 干预措施
Active treatment
Other
干预措施: Viveve System (Device)
结局指标
主要结局
Safety - Adverse Events
时间窗: baseline to 6 month
safety of treatment of female sexual dysfunction secondary to SSRI sexuality syndrome
次要结局
- Female Sexual Function Index (FSFI)(baseline to 3 and 6 months)
研究者
Michael Krychman, MD
Michael Krychman, MD
Southern California Center for Sexual Health and Survivorship Medicine
研究点 (2)
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