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临床试验/NCT00188071
NCT00188071已完成不适用

Postoperative Pain After Medical Abortion Under Local Anesthesia : a Prospective and Randomized Trial Comparing Several Analgesic Regimen

University Hospital, Angers2 个研究点 分布在 1 个国家目标入组 240 人开始时间: 2002年9月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
240
试验地点
2
主要终点
postoperative pain rating

研究概览

简要总结

  • To compare postoperative analgesia by paracetamol 1gr or ketoprofen 100 mg or the combination of these two analgesics
  • each treatment beeing allocated by randomization

详细描述

  • 240 pregnant women who undewent a medical abortion by aspiration, under local anesthesia, (day case surgery) were enrolled after informed consent and signed approval

  • according to randomization, they received one hour before medical abortion procedure performed under local anesthesia of the cervix, one of these three diffrente analgesics :

  • paracetamol 1 gr

  • ketoprofen 100 mg

  • the association of both Postprocedure pain was recorded, by nurse, using a visual analog scale (VAS), 7 times before and after the procedure, until the discharge of the patient.

  • if VAS was above 40 on two consecutive measurements a morphine injection was given.

  • the number and total amount of morphine was recorded.

  • satisfaction was recorded within the 3 postoperative day by a telephone inquiry.

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
Single

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • pregnant women
  • medical abortion performed in day case surgery under local anesthesia
  • informed written consent

排除标准

  • under 18 year old

结局指标

主要结局

postoperative pain rating

次要结局

  • morphine consumption
  • patient satisfaction

研究者

发起方
University Hospital, Angers
申办方类型
Other Gov

研究点 (2)

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