ISRCTN02384619已完成不适用
A double blind randomised placebo-controlled trial to compare the effectiveness of paracervical block plus Intrauterine anesthesia and paracervical block alone for pain relief during fractional durettage
Mahidol University - Siriraj Grant for Research Development (Thailand)0 个研究点目标入组 70 人开始时间: 2005年7月8日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 70
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
- 性别
- Female
入选标准
- •Women with abnormal uterine bleeding scheduled for fractional curettage.
排除标准
- •Patients who had the American Society of Anesthesiologists (ASA) physical status >II, genital organ infection, profuse uterine bleeding, a history of lidocaine hypersensitivity, a history of impaired liver function, were virgin, pregnant, or unable to understand how to score a 10-cm visual analogue scale (VAS) pain score.
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