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临床试验/NCT00815503
NCT00815503已完成4 期

Postoperative Analgesia With Local Infiltration After Periacetabular Osteotomy For The Treatment Of Dysplasia

Odense University Hospital1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2009年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
70
试验地点
1
主要终点
Consumption of rescue analgetics

研究概览

简要总结

Pain treatment after periacetabular osteotomy is traditionally based on systemic opioids wich have side effects. The purpose of this study is to evaluate the analgetic effect of wound infiltration with local anaesthesia after periacetabular osteotomy.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Periacetabular osteotomy due to traditional dysplasia or retroverted acetabulum
  • Informed consent

排除标准

  • Intolerance of local anaesthesia
  • Habitual use of opioids

研究组 & 干预措施

Ropivacaine

Active Comparator

干预措施: Ropivacaine (Drug)

Saline

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Consumption of rescue analgetics

时间窗: Assesment of opioid rescue analgetics every 24 hours for 14 days postoperatively

次要结局

  • Pain(Assessment of pain four times every day for five days postoperatively)

研究者

申办方类型
Other

研究点 (1)

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