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临床试验/NCT01149616
NCT01149616终止4 期

Effects of Perioperative Intravenous Dexamethasone on Pain in Out Patient Knee Surgery

Beth Israel Deaconess Medical Center1 个研究点 分布在 1 个国家目标入组 82 人开始时间: 2009年12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
终止
入组人数
82
试验地点
1
主要终点
Post Operative VAS Pain Scale

研究概览

简要总结

The purpose of the study is to determine the opiate sparing effects of intravenously administered dexamethasone in outpatient knee surgery. Dexamethasone is a glucocorticoid with well known antiemetic effects. However, the analgesic effects of dexamethasone have not been adequately researched. Following surgery, patients are typically discharged home with PO opiates to manage post-operative pain. The investigators believe that by using VAS (Visual Analog Scale) for Pain the investigators can show that a single dose of dexamethasone can reduce pain scales and opiate consumption post-operatively, on Post Operative Day (POD 1) when compared to placebo.

详细描述

Findings of Modest improvement in pain scores and postoperative nausea at 24 hours with Dexamethasone

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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients undergoing ambulatory knee arthroscopy surgery
  • Must provide phone contact number and agree to phone followup on post operative day 1

排除标准

  • Patients with major systemic disease
  • Allergy or intolerance to study drug

研究组 & 干预措施

Intervention

Active Comparator

Dexamethasone 8mg iv x 1

干预措施: Dexamethasone 8mg iv x1 (Drug)

Placebo

Placebo Comparator

placebo

干预措施: placebo (Drug)

结局指标

主要结局

Post Operative VAS Pain Scale

时间窗: 24 hours

Patients were instructed to select a number between zero and ten to indicate the degree of pain they experience (zero being no pain and ten being the worst pain they could imagine). Therefore, ten is worse than zero.

次要结局

  • Amount of Postop Narcotic Usage(24 hours)
  • Postop Nausea(24 hours)

研究者

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

Lauren J. Fisher

Attending Physician

Beth Israel Deaconess Medical Center

研究点 (1)

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