跳至主要内容
临床试验/ACTRN12614000860662
ACTRN12614000860662招募中不适用

Post-operative analgesic efficacy of dexamethasone sodium phosphate versus triamcinolone acetonide in bunion surgery: A prospective, single-blinded randomized controlled trial

niversity of Western Australia0 个研究点目标入组 25 人开始时间: 2014年8月11日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
25

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • 1.Undergoing surgical correction of hallux valgus facilitated through the UWA Podiatric Surgery Clinic
  • 2.Aged 18 years or older

排除标准

  • 1.Cognitive impairment, intellectual disability, physical disability or mental illness
  • 2.Allergy/ hypersensitivity to any corticosteroids
  • 3.Systemic viral and fungal infections
  • 4.Allergy/ hypersensitivity to Prodeine - Registered Trademark 15
  • 5.Diabetes mellitus, inflammatory arthritis and any other forms of immunodeficiency
  • 6.Currently taking medications that can interact with dexamethasone sodium phosphate or triamcinolone acetonide

研究者

发起方
niversity of Western Australia

相似试验