NCT06540599已完成4 期
Optimizing Analgesia for Endometrial Biopsy: A Prospective, Randomized Comparative Study
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 197
- 试验地点
- 1
- 主要终点
- comparing analgesics in endometrial biopsy using The Visual Analogue Scale (VAS).
研究概览
简要总结
Comparison of the effectiveness of intrauterine lidocaine-paracervical block-dexketoprofen tromematol- lidocaine spray in endometrial biopsy analgesia
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 75 Years(Adult, Older Adult)
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •women aged 18-75 needs endometrial biopsy
排除标准
- •women with allergies to prilocaine, lidocaine or dexketoprofen trometamol
- •women with a history of severe uncontrolled cardiovascular disease, diabetes mellitus, pregnancy, vaginal, cervical, or pelvic infection, cervical cancer, or severe cervical stenosis
研究组 & 干预措施
Patients using intrauterine lidocaine for analgesia
Active Comparator
干预措施: Analgesic (Drug)
Patients using oral dexketoprofen for analgesia
Active Comparator
干预措施: Analgesic (Drug)
Patients using cervical lidocaine spray for analgesia
Active Comparator
干预措施: Analgesic (Drug)
Patients using paracervical block with prilocaine for analgesia
Active Comparator
干预措施: Analgesic (Drug)
结局指标
主要结局
comparing analgesics in endometrial biopsy using The Visual Analogue Scale (VAS).
时间窗: 1 hour
post operative VAS scores will be compared for each drug.The VAS measures pain intensity. The VAS consists of a 10 cm line, with two end points representing 0 ('no pain') and 10 ('pain as bad as it could possibly be'). In this context, higher scores represent worse results.
次要结局
未报告次要终点
研究者
研究点 (1)
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