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临床试验/NCT00799162
NCT00799162Unknown不适用

Prediction of Post-Cesarean Section Pain

University of Washington5 个研究点 分布在 4 个国家目标入组 800 人开始时间: 2008年11月最近更新:
适应症

试验速览

阶段
不适用
入组人数
800
试验地点
5

研究概览

简要总结

The purpose of this study is to determine if dynamic psychophysical testing along with genetic screening will allow to identify pre-operatively women who will suffer severe acute pain post-operatively and the subset who may experience chronic pain following cesarean section.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Women age 18-50 scheduled for an elective cesarean section (1st or 2nd cesarean section)

排除标准

  • have taken opioids, acetaminophen, or NSAIDs 48 hrs prior to psychophysical testing
  • have had more than two previous cesarean sections
  • have a vertical abdominal incision from a prior cesarean section
  • are non-English speaking
  • have mental health issues
  • have a failure of spinal anesthetic and require conversion to general anesthesia
  • have a vertical uterine incision performed during ongoing cesarean section
  • have a previous vertical uterine scar discovered during ongoing cesarean section

研究者

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

Ruth Landau

Professor

University of Washington

研究点 (5)

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