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临床试验/TCTR20230621006
TCTR20230621006招募中2 期

se of Vaginal Misoprostol to Relieve Pain During Operative Hysteroscopy in Office Setting: A Randomized Double-Blinded Placebo Controlled Study

/A0 个研究点目标入组 78 人开始时间: 2023年6月21日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
78

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 50 Years(—)
性别
Female

入选标准

  • 1 Women who had an appointment for operative hysteroscopy in outpatient department at ramathibodi hospital
  • 2 age 18-50 years and in reproductive age
  • 3 pelvic examination can done
  • 4 BMI 18-30 kg/m2
  • 5 Have confirm test from ultrasound or diagnostic hysteroscopy that have intrauterine lesion that require surgery such as endometrial polyp, myoma uteri size less than 3 cm., intrauterine adhesion, uterine septum, foreign body
  • 6 Be willing to participate in the research and sign a consent letter

排除标准

  • 1 Have contraindication for hysteroscopy such as pregnancy, pelvic inflammatory disease, suscepted cervical cancer or advance stage endometrial cancer
  • 2 Underlying disease such as asthma, chronic kidney disease or hepatitis
  • 3 Allergy to Misoprostol, NSIADs
  • 4 Cervical stenosis or history cervical operation

研究者

发起方
/A

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