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临床试验/NCT00374504
NCT00374504已完成不适用

Prediction of Postoperative Pain by an Electrical Pain Stimulus

Rigshospitalet, Denmark1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2006年9月11日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
46
试验地点
1

研究概览

简要总结

The aim of this study is to evaluate a possible correlation between predictive precesarean section pain and development of postcaesarean section pain using the PM.

Patients and Methods 46 healthy pregnant women scheduled for elective cesarean section is included after informed consent. The standard operation procedures included spinal anesthesia, paracetamol 1 g 8 hourly, diclofenac 50 mg 8 hourly and oxycontine 10 mg x 2. Morphine was used for break-through pain.

Before cesarian section the threshold for sensory and pain were measured 3 times, and the average was used for analyses. After cesarian section a blinded midwife assess the pain at rest and during mobilization every 12th hours over 2 days score.

Data was analyzed using AUC and non-parametric test, P < 0,05.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

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

  • Healthy pregnant women scheduled for elective cesarean section

排除标准

  • ASA III -IV
  • Chronic pain conditions.
  • Pacemaker.

研究者

申办方类型
Other

研究点 (1)

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