跳至主要内容
临床试验/NCT02210429
NCT02210429已完成不适用

Supraclavicular Blocks for Post-Operative Pain Control in Supracondylar Fracture Fixation, a Retrospective Analysis of Single Shot Catheter Techniques

Ann & Robert H Lurie Children's Hospital of Chicago1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2009年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
200
试验地点
1
主要终点
Post-operative opioid use

研究概览

简要总结

We hypothesize that patients who receive a supraclavicular block via Angiocath, placed intra-operatively and dosed post-operatively following neurologic examination, will have lower pain scores, lower use of intravenous morphine equivalents in the post-anesthesia care unit, and lower rates of intervention for post-operative nausea and vomiting. We also hypothesize that patients receiving this nerve block had the same rates of nerve damage as the patients who did not receive a block and that there will be no demonstrable safety concerns with this block.

研究设计

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

入排标准

年龄范围
— 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Age under 18
  • Undergoing supracondylar fracture fixation in operating room

排除标准

  • Incomplete or inaccessable chart data

研究组 & 干预措施

Supraclavicular Catheter

Active Comparator

干预措施: Elbow Fracture Fixation (Procedure)

Supraclavicular Angiocath

Active Comparator

干预措施: Elbow Fracture Fixation (Procedure)

IV Opioids

Active Comparator

干预措施: Elbow Fracture Fixation (Procedure)

Supraclavicular Single-Shot Block

Active Comparator

干预措施: Elbow Fracture Fixation (Procedure)

结局指标

主要结局

Post-operative opioid use

时间窗: 24 hours

Total doses

次要结局

  • Pain Score(24 hours)
  • Anti-emetic drug use(24 hours)
  • Incidence of nerve damage or compartment syndrome(1 month)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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