跳至主要内容
临床试验/TCTR20240620003
TCTR20240620003尚未招募4 期

idocaine gel combined with ibuprofen versus ibuprofen alone for pain relief during an endometrial biopsy; A randomized controlled trial.

Khon Kaen Hospital0 个研究点目标入组 100 人开始时间: 2024年6月20日最近更新:
适应症

试验速览

阶段
4 期
状态
尚未招募
入组人数
100

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 N/A (No limit)(—)
性别
Female

入选标准

  • 1.Age >=18 years old.
  • 2. Women who had an indication for an endometrial sampling: abnormal uterine bleeding in age >=35 years, age < 35 years with risk factors (history of unoppsed estrogen exposure, failed medical management, persistent abnormal uterine bleeding), abnormal uterine bleeding with tamoxifen taking, postmenopausal bleeding.

排除标准

  • 1.Previous history of lidocaine allergy.
  • 2.Previous history of NSAIDs allergy.
  • 3.Previous history of sulfa drugs allergy.
  • 4.History of gastric ulcer, gastritis, gastrointestinal bleeding.
  • 6.Uncontrolled hypertension.
  • 7.Bleeding disorder.
  • 8.Kidney disease.
  • 9.Liver disease.
  • 10.G6PD deficiency.
  • 11.Cardiac arrhythmias.
  • 12.Coronary heart disease.
  • 13.Uterine anomaly.
  • 14.Massive vaginal bleeding.
  • 15.Recieves misoprostol for cervical dilation.
  • 16.Inability to give consent or participant in postoperative assessment owing to dementia, cognitive impairment or language barrier.
  • 17. Unable to use visual analogue scale (VAS).
  • 18. Ongoing vagina or cervix or pelvic infection.
  • 19.Combination with endocervical biopsy.
  • 20.Cervical stenosis.
  • 21.Cannot pass instrument into endometriod cavity.

研究者

相似试验