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临床试验/NCT07630896
NCT07630896尚未招募4 期

Postoperative Prednisone Regimen in TKA and Its Effect on Continuous Glucose Levels

Columbia University1 个研究点 分布在 1 个国家目标入组 104 人开始时间: 2026年7月1日最近更新:
适应症

试验速览

阶段
4 期
状态
尚未招募
入组人数
104
试验地点
1

研究概览

简要总结

This study compares the efficacy of a 5-day post-operative oral prednisone regimen (40 mg daily) with the standard intraoperative steroid regimen, focusing on pain, swelling, range of motion, opioid use, and glucose levels monitored continuously.

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
None

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

  • Undergoing Primary Unicompartmental Knee Arthroplasty or Total Hip Arthroplasty
  • Age 18 and above

排除标准

  • Steroid therapy
  • Narcotic use within past 3 months
  • History of corticosteroid intolerance
  • Pregnancy
  • Uncontrolled diabetes
  • Doesn't own smart phone
  • Drop Criteria:
  • - 2nd dose of IV dexamethasone

研究者

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

Roshan P. Shah

Russell A. Hibbs Associate Professor of Orthopedics in Orthopedic Surgery and in Surgery

Columbia University

研究点 (1)

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