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临床试验/KCT0005586
KCT0005586招募中未知

A multi-center, randomized, investigator-initiated trial to evaluate the efficacy of PRreservation of ovArian function, Hemostasis, and sAfety of a hemostatic agent versus suturing during laparoscopic ovarian cystectomy for ovarian endometriosis

Seoul National University Hospital0 个研究点目标入组 90 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
90

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19(Year) 至 45(Year)(—)
性别
Female

入选标准

  • Informed consent.
  • Age: 19-45 year-old women
  • American Society of Anesthesiologists Physical Status classification 1 or 2
  • Plan of laparoscopic ovarian cystectomy for unilateral or bilateral ovarian endometriosis diagnosed by ultrasonography
  • Regular menstruation every 21-45 days

排除标准

  • No ‘ovarian’ endometriosis
  • Suspicious disease of ovarian malignancy
  • Age: 18 and younger, 46 and older
  • Pregnancy or breastfeeding.
  • Lower than 0.05 ng/ml of serum Anti-mullerian hormone level
  • Hormonal therapy within recent 3 months
  • Considered as inappropriate by the researcher's judgment.

研究者

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Comparison of hemostatic agent to suture in terms of... | 临床试验