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临床试验/NCT01414569
NCT01414569已完成4 期

High Dose Dexamethasone as Pain Treatment After Arthroscopic Shoulder Surgery: A Randomised, Blinded Clinical Trial

University of Aarhus1 个研究点 分布在 1 个国家目标入组 97 人开始时间: 2011年11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
97
试验地点
1
主要终点
Pain score by numeric rating scale

研究概览

简要总结

The purpose of this study is to determine if a dose of 40 mg dexamethasone is more effective as pain treatment than the currently used dose of 8 mg after arthroscopic shoulder surgery.

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

入选标准

  • Arthroscopic subacromial decompression and/or acromioclavicular resection
  • General anaesthesia
  • Daysurgery, Horsens Hospital

排除标准

  • Incompetent
  • Age under 18 or over 90 years
  • Allergy toward dexamethasone
  • Active gastric ulcer
  • Untreated hypertension
  • Daily use of glucocorticoids or strong opioids
  • Daily use of analgesics for unrelated illness
  • Myasthenia gravis
  • Mitochondrial disorders

研究组 & 干预措施

8 mg dexamethasone

Active Comparator

干预措施: Dexamethasone (Drug)

Placebo, saline

Placebo Comparator

干预措施: Dexamethasone (Drug)

40 mg dexamethasone

Experimental

干预措施: Dexamethasone (Drug)

结局指标

主要结局

Pain score by numeric rating scale

时间窗: At 8 hours postoperatively

次要结局

  • Use of analgesics(During hospital stay, about 4 hours)
  • Pain score by numeric rating scale(At about 8 a.m. on the first postoperative day)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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