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临床试验/NL-OMON56651
NL-OMON56651尚未招募不适用

Sexual function in women with prior severe preeclampsia. - S-FUPEC

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 122 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
122

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 64(—)

入选标准

  • - Being in between 9-15 months postpartum
  • - Aged above 18 years
  • - Being in a stable relationship for at least 6 months
  • - Diagnosis of severe preeclampsia, based on the ACOG definition or healthy
  • postpartum women without a history of severe preeclampsia.

排除标准

  • - Pregnant women
  • - Having undergone a radical hysterectomy or prolapse surgery
  • - Usage of medications that are known to influence sexual response, with the
  • exception of contraceptive use.
  • - Medical disorders (other than a history of preeclampsia) that are known to
  • influence sexual response, such as heart failure or chronic obstructive
  • pulmonary disease.

研究者

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