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临床试验/NCT02709590
NCT02709590已完成3 期

Randomized Clinical Trial of Oral Diclofenac Potassium With Cervical Lidocaine Cream in Reducing Pain During HSG

Assiut University1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2016年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
140
试验地点
1
主要终点
Mean pain score during hysterosalpigography by visual analog scale

研究概览

简要总结

The aim of our study is to determine the efficacy of oral diclofenac potassium combined with lidocaine cream on the pain scores during HSG.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Care Provider)

入排标准

年龄范围
19 Years 至 42 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • any patient came for HSG

排除标准

  • any patient has contraindication to HSG

研究组 & 干预措施

Group A

Experimental

oral diclofenac potassium plus lidocaine anesthetic cream placed into their cervix immediately before HSG

干预措施: diclofenac potassium + lidocaine (Drug)

Group B

Placebo Comparator

oral placebo tablets plus placebo cream placed into their cervix immediately before HSG

干预措施: placebo (Drug)

结局指标

主要结局

Mean pain score during hysterosalpigography by visual analog scale

时间窗: intraoperative

次要结局

  • Mean pain score after hysterosalpigography(30 minutes)
  • side effects of medication(30 minutes)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ahmed Mohamed Abbas

Dr

Assiut University

研究点 (1)

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