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临床试验/NCT00308841
NCT00308841已完成1 期

Anesthetic Efficacy of Intrauterine Lidocaine for Removal of a "Lost" Intrauterine Device

Suleyman Demirel University2 个研究点 分布在 2 个国家开始时间: 2006年3月30日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
已完成
试验地点
2

研究概览

简要总结

Objective: To evaluate the efficacy of intrauterine lidocaine instillation in reducing patient discomfort during the removal of a "lost" intrauterine device (IUD).

Methods: This double-blinded, randomized, placebo-controlled trial included 68 women who underwent removal procedure for a "lost" IUD. Thirty-four women were allocated to the lidocaine group and 34 to the saline group. The main outcome measure was the intensity of pain during, immediately after, and 20 minutes after the procedure, assessed by a visual analog scale. Statistical analysis was performed using Friedman's test with Bonferroni correction, Student's t test, and 2.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Double

入排标准

性别
Female
接受健康志愿者

入选标准

  • patients undergoing a minor gynecologic procedure for removal of a "lost" IUD.

排除标准

  • women with a history of cervical stenosis, known allergy to lidocaine, pregnancy, acute cervicitis

研究者

申办方类型
Other

研究点 (2)

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