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临床试验/NCT02317601
NCT02317601已完成4 期

Preoperative Single-high Dose Glucocorticoid for Patients Undergoing Hip Fracture Surgery and the Effect on Postoperative Delirium.

Hvidovre University Hospital1 个研究点 分布在 1 个国家目标入组 122 人开始时间: 2014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
已完成
入组人数
122
试验地点
1
主要终点
Post operative delirium measured with Confusion Assessment Method severity measure CAM-S

研究概览

简要总结

The Study is a double-blinded, randomized, placebo-controlled trials. The Objective is to investigate the effect of single-high-dose glucocorticoid on surgical stress response and postoperative delirium among Elderly hip Fracture Patients undergoing surgery.

详细描述

Patients with Hip Fracture are exposed for two traumas that can trigger a stress response. The first is the fall that causes the Fracture. The second is the surgery. In this study the intervention is dispensed early in the disease course - as soon as the Fracture has been diagnosed and booked for surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients undergoing surgery for hip fracture
  • Informed signed consent
  • Danish speaking

排除标准

  • Allergies towards contents of Solu-Medrol
  • Insulin dependent diabetes
  • In treatment for cancer disease
  • Positive HIV, Hepatitis b or C status
  • Lack of informed consent (eq. Severe dementia, coma, and others)
  • Current treatment with systemic glucocorticoids (pr.os or intravenous) Immunoinflammatory disease (Except topical treated skin disease and respiratory disease)
  • Current Immunosuppressive treatment
  • Unable to participate in CAM-S measurement
  • Peptic ulcera

研究组 & 干预措施

Methylprednisolone sodium succinate

Active Comparator

125 mg iv, as single dose, preoperative.

干预措施: methylprednisolone sodium succinate (Drug)

physiological saline

Placebo Comparator

5 mL of Sodium-Chloride 9 mg/ml, Fresenius Kabi

干预措施: placebo saline (Drug)

结局指标

主要结局

Post operative delirium measured with Confusion Assessment Method severity measure CAM-S

时间窗: 3 first post operative days

Post operative delirium measured with Confusion Assessment Method severity measure CAM-S

次要结局

  • Post operative delirium incidents measured by CAM-S(3 days)
  • Patient mobility measured by Cumulated Ambulation Score (CAS)(3 first operative days)
  • The degree of inflammatory response measured by biomarker in the blood (suPAR, Interleukin 6, and others)(4 days)
  • Post operative Fatigue measured with a patient fatigue self-assessment 0-4. (Verbal rating scale) 0=no fatigue, 1=mild, 2 = moderate, 3 = severe, 4 = excruciating (in bed because of fatigue).(3 first postoperative days)
  • Psychiatric medications (total amount/use of psychiatric medications)(3 post-OR days)
  • Postoperative infections (numbers of patients with postoperative infections)(21 days)
  • Length of stay in hospital(21 days)

研究者

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

Christopher Clemmesen

MD

Hvidovre University Hospital

研究点 (1)

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