TCTR20180815004尚未招募未知
10% Lidocaine spray for pain control during intrauterine device insertion in nulliparous women: A randomized, double-blinded, placebo controlled Trial
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 124
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 45 Years（—）
- 性别
- Female
入选标准
- •Woman who required for Copper T IUD insertion
- •Age 18-45 years
- •New IUD user
- •Body mass index 18.5 †30 kg/m2
- •Communicable with Thai language
排除标准
- •Suspicion of pregnancy
- •Puerperal sepsis/Immediate post-septic abortion
- •Untreated abnormal uterine bleeding
- •Uterine anomaly/abnormal pathology distorting the uterine cavity
- •Current pelvic inflammatory disease
- •Untreated cervicitis/vaginitis
- •Wilson’s disease
- •Copper allergy
- •known hypersensitivity to local anaesthetics.
- •Analgesic or anxiolytic use within the last 24 h before the procedure
研究者
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