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临床试验/NCT02445898
NCT02445898已完成2 期

Effect of Preoperative Intravenous High Dose Methylprednisolone on Orthostatic Intolerance and Heart Rate Variability in Patients Scheduled for Total Hip-arthroplasty

Rigshospitalet, Denmark1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2015年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
64
试验地点
1
主要终点
Difference in incidence of orthostatic intolerance from baseline to 6 hours after surgery

研究概览

简要总结

The study evaluates the pathophysiological effects of a single dose Methylprednisolone administered prior to total hip-arthroplasty (THA) surgery. The investigators examine the effect on orthostatic intolerance, orthostatic hypotension and heart rate variability (HRV) to evaluate the efficacy of Methylprednisolone regarding blood pressure regulation and autonomic responses after THA.

Half of participants will receive intravenous Solu-Medrol 125 mg, while the other half will receive placebo.

The investigators hypothesize that the group receiving Methylprednisolone will be less orthostatic intolerant, experience less orthostatic hypotension and have an improved autonomic response compared to the placebo-group, early after THA.

详细描述

The anti-inflammatory effects of glucocorticoids are well known. The beneficial effects in postoperative pain, postoperative nausea and vomiting are well-documented.

Hip-arthroplasty surgery and the inflammatory stress response in general affect the potential of recovery. Early postoperative orthostatic intolerance is common in patients undergoing THA with an incidence of 40%. The mechanism is thought related to an impaired autonomic regulation caused by surgery-induced inflammation. The effect of glucocorticoids on orthostatic intolerance, orthostatic hypotension and HRV after hip-arthroplasty surgery is unknown and calls for further investigation.

The study is to be considered as exploratory. The primary analysis of the primary outcome measure is a comparison of the incidence of orthostatic intolerance from baseline to 6 hours postoperatively between the two groups.

For calculation of sample size the difference in incidence between groups (40% versus 10%) from baseline (before surgery) to 6 hours after THA-surgery, a risk of type I errors 5% and a risk of type II errors 20% (80% power) were used.

The primary analysis is carried out on all included patients (intention-to-treat) with baseline values as covariate. Secondary exploratory per-protocol analysis might be performed. Missing outcomes will be analysed using multiple imputation due to expected strong time trends.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
55 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Osteoarthrosis
  • Undergoing total unilateral hip-arthroplasty surgery
  • Speak and understand Danish
  • Have given informed content

排除标准

  • Revision or bilateral hip-arthroplasty surgery
  • General anaesthesia
  • Allergy or intolerance towards Methylprednisolone
  • Local or systemic infection
  • Permanent systemic treatment with steroids within 30 days peroperatively
  • Insulin-dependent diabetes
  • Atrial fibrillation
  • Neurological disease incl. Parkinsons
  • Daily use of hypnotics or sedatives
  • Alcohol abuse >35 units per week
  • Active treatment of ulcer within 3 months preoperatively
  • Cancer disease
  • Autoimmune disease incl. rheumatoid arthritis
  • Pregnant or breast feeding women
  • Menopause <1 year

研究组 & 干预措施

Methylprednisolone

Active Comparator

Preoperative single high dose of Solu-Medrol 125 mg iv.

干预措施: Methylprednisolone (Drug)

Isotonic Sodium Chloride

Placebo Comparator

Preoperative single dose of isotonic Sodium Chloride

干预措施: Isotonic Sodium Chloride (Drug)

结局指标

主要结局

Difference in incidence of orthostatic intolerance from baseline to 6 hours after surgery

时间窗: 6 hours after surgery

次要结局

  • Change in systemic vascular resistance from baseline to 24 hours after surgery(24 hours after surgery)
  • Change in pain intensity from baseline to 24 hours after surgery(24 hours after surgery)
  • Change in concentration of C-reactive protein from baseline to 48 hours after surgery(48 hours after surgery)
  • Difference in incidence of orthostatic intolerance from baseline to 24 hours after surgery(24 hours after surgery)
  • Change in non-invasive blood pressure from baseline to 24 hours after surgery(24 hours after surgery)
  • Change in heart rate variability from baseline to 24 hours after surgery(24 hours after surgery)
  • Change in stroke volume and cardiac output from baseline to 24 hours after surgery(24 hours after surgery)
  • Change in concentration of plasma-hemoglobin from baseline to 48 hours after surgery(48 hours after surgery)

研究者

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

Viktoria Oline Lindberg-Larsen

MD, PhD student

Rigshospitalet, Denmark

研究点 (1)

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