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临床试验/NCT03014765
NCT03014765已完成不适用

Endothelial Dysfunction, Indicator of Perioperative Complications and Its Changes in Perioperative Period

University Medical Centre Ljubljana0 个研究点目标入组 70 人开始时间: 2017年1月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
70
主要终点
rate of perioperative cardiovascular complications in patients scheduled for hip arthroplasty under spinal anesthesia related to endothelial dysfunction

研究概览

简要总结

Study will enroll patients scheduled for hip arthroplasty. In each subject a flow-mediated dilatation capability (FMD) of the brachial artery will be measured prior to elective surgery, within 24 hours after surgery and 5-7 days after surgery. At each session the brachial artery diameter will be measured at rest, during cuff inflation and 50 seconds after cuff deflation. From above mentioned values the increase in the diameter of the artery during reactive hyperemia will be calculated.

Simultaneously with the ultrasound investigations, the blood for determination of the endothelial dysfunction markers will be collected.

The participants will be contacted again 3 months after the surgery and asked about the complications which may be associated with the surgery.

详细描述

Cardiovascular complications, especially coronary heart disease, are one of the main causes of perioperative complications. Indicators of pre-clinical atherosclerosis, such as: endothelial dysfunction, increased arterial intima/media thickness (especially in the carotid arteries), carotid calcification and coronary calcification, suggest the presence of atherosclerotic process without the symptomatic presentation. Endothelial dysfunction is one of the earliest measurable changes that predict the development of atherosclerotic disease.

Surgery is a significant stress for the organism: it increases the release of free oxygen radicals and through oxidative stress it increases systemic inflammatory response and causes thromboembolic complications.

In the study 50 patients of both sexes 40-80 years of age scheduled for hip arthroplasty will be included. In each subject a flow-mediated dilatation capability (FMD) of the brachial artery will be measured prior to elective surgery, within 24 hours after surgery and 5-7 days after surgery. Measurement of the brachial artery flow-mediated dilatation capability (FMD): the brachial artery diameter will be measured 5 cm proximal to the antecubital fossa at rest, during cuff inflation and 50 seconds after cuff deflation. The cuff will be inflated for 4 min. From above mentioned values the increase in the diameter of the artery during reactive hyperemia will be calculated.

Simultaneously with the ultrasound investigations, the blood for determination of the inflammatory and endothelial dysfunction markers (CRP, IL-6, IL-8, IL-10, IL-18, TNFa, VW Factor, Selectin P, selectin E) will be collected.

The participants will be contacted again 3 months after the surgery and asked about the complications which may be associated with the surgery.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

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

入选标准

  • •scheduled hip arthroplasty under spinal anesthesia

排除标准

  • •Acute coronary syndrome or cerebrovascular syndrome in the last 6 months
  • •Acute venous thrombosis in the last 6 months
  • •Episode of rheumatoid arthritis in the last 3 months or permanent therapy with prednisolone >4mg/day
  • •Acute illness or hospitalization in the last month
  • •Chronic kidney failure on dialysis
  • •Hepatic failure
  • •Active malignant disease
  • •Immunosuppression after organ transplantation
  • •Pregnancy
  • •No informed consent after oral and written information

结局指标

主要结局

rate of perioperative cardiovascular complications in patients scheduled for hip arthroplasty under spinal anesthesia related to endothelial dysfunction

时间窗: 12 months

次要结局

  • levels of blood circulating markers of increased perioperative stress and systemic inflammatory response(12 months)
  • decrease in endothelial function(12 months)

研究者

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

Peter Poredos

Head of Orthopaedic Anaesthesia

University Medical Centre Ljubljana

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