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临床试验/NCT01753258
NCT01753258已完成不适用

Outcomes of Delivery in Patients With Dyspareunia- A Prospective Study

Hadassah Medical Organization1 个研究点 分布在 1 个国家目标入组 173 人开始时间: 2013年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
173
试验地点
1
主要终点
Obstetrical outcome of women with a history of dyspareunia

研究概览

简要总结

The focus of this pilot study is to determine if a woman who experiences pain during sexual intercourse has a higher risk of complications during labor and delivery secondary to pelvic floor dysfunction, anxiety and intolerance towards pelvic examinations. Furthermore, it is unclear whether women with prepartum dyspareunia experience an improvement following vaginal delivery. While physicians may expect that vaginal birth improves dyspareunia due to the stretching effect on pelvic floor, to date, there is insufficient evidence to support this claim. The Investigators plan to prospectively study 200 patients at our Institution, collect information regarding birth and follow them, via questionnaires, regarding their dyspareunia postpartum.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 200 nulliparous women admitted to the Labor and Delivery Department at the Hadassah Medical Center, above the age of
  • Able and willing to read, understand, and sign the Informed Consent Form and questionnaire.
  • Agree to be contacted in the future to complete telephone questionnaires.

排除标准

  • Induction of labor
  • Placental abruption, placenta previa
  • Malpresentation
  • Non reassuring fetal heart rate upon admission
  • Any other contraindication for vaginal delivery
  • Multifetal pregnancy

结局指标

主要结局

Obstetrical outcome of women with a history of dyspareunia

时间窗: 3 months -1 year

The Investigators will record the mode of delivery (vaginal, instrumental or cesarean section), length of the second stage of labor, use of anesthetics, perineal tears and\\or episiotomies, and newborn's birth weight. The evaluation will be done prospectively, comparing data with matched controls without a history of dyspareunia.

次要结局

  • Rate of alleviation of dyspareunia following vaginal delivery as assessed through patient questionnaires.(2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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