NCT01402791已完成不适用
Endometriosis: Sexual Dysfunction and Adaptation Strategies Among Couples
Centre Hospitalier Universitaire de Nīmes1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2011年1月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Score for the IIEF questionnaire
研究概览
简要总结
The primary objective of this study is to evaluate the presence/absence and description of persistent sexual troubles following surgical treatment for endometriosis for women, and their partners.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •The patient (and her partner) must have given his/her informed and signed consent
- •The patient (and her partner) must be insured or beneficiary of a health insurance plan
- •Couples for whom the woman has formerly undergone surgical treatment for endometriosis, and for the partner agrees to respond to questionnaires for this study
排除标准
- •The patient (or her partner) is participating in another study
- •The patient (or her partner) is in an exclusion period determined by a previous study
- •The patient (or her partner) is under judicial protection, under tutorship or curatorship
- •The patient (or her partner) refuses to sign the consent
- •It is impossible to correctly inform the patient (or her partner)
- •The patient is pregnant
- •The patient is breastfeeding
- •The patient was surgically treated for endometriosis, but was single.
结局指标
主要结局
Score for the IIEF questionnaire
时间窗: Day 1
Score for the IIEF questionnaire; varies from 0 to 75.
Score for the SFQ questionnaire
时间窗: Day 1
Score for the SFQ questionnaire; varies from 0 to 5.
次要结局
- Scores for each sub-domain of the SFQ questionnaire(Day 1)
- Scores for each sub-domain of the IIEF questionnaire(Day 1)
- Sexual treatment request (yes/no)(Day 1)
研究者
研究点 (1)
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