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临床试验/NCT03953573
NCT03953573已完成不适用

Management of Post-delivery Pain and Its Impact on Resumption of Sexuality

Hopital Foch1 个研究点 分布在 1 个国家目标入组 105 人开始时间: 2018年12月22日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Hopital Foch
入组人数
105
试验地点
1
主要终点
Post-delivery sexuality resumption

研究概览

简要总结

Study of management of pain and information given to women post-delivery and their impact of the resumption of sexuality.

Survey to be completed by women at 8 and 15 days and 1 or 3 months after delivery.

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 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Primiparous woman
  • Age between 18 and 45 years old
  • Delivery after 37 weeks of amenorrhea
  • Speaking French
  • Pregnancy, delivery and new-born examination without morphologic or biometric abnormalities, respiratory distress and no pathology discovered at neonatal screening on day 3
  • Heterosexual woman with partner
  • Signed consent
  • Affiliate of national health insurance scheme

排除标准

  • Multiple pregnancy,
  • BMI > 30
  • Conjugopathie
  • Known psychiatric history
  • Medical history with gynecologic impact
  • Surgery history with gynecologic impacts
  • Hysterectomy post-delivery
  • Protected by French law

结局指标

主要结局

Post-delivery sexuality resumption

时间窗: 3 months

Time to sexuality resumption

次要结局

  • Sexual health(3 months)
  • Pain post-delivery(3 months)
  • Discussion with healthcare professional on post-delivery sexuality(1 month)

研究者

发起方
Hopital Foch
申办方类型
Other
责任方
Sponsor

研究点 (1)

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