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临床试验/NCT00431691
NCT00431691已完成4 期

Effect of Antioxidants on Ocular Blood Flow, Endothelial Function, and Cytokine Levels in LPS Induced Inflammatory Model in Humans.

Medical University of Vienna1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2006年9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
22
试验地点
1
主要终点
Retinal blood flow

研究概览

简要总结

Oxidative stress, which refers to cellular damage caused by reactive oxygen intermediates, has been implicated in many disease processes, especially age-related disorders. Many trials investigating use of antioxidants in protecting different tissues against oxidative stress have been conducted, but the results are ambiguous.

Inflammation is generally associated with enhanced oxidative stress and widespread endothelial dysfunction. In the present study, the infusion of LPS, which is a cell wall component of Gram-negative bacteria and a major mediator in the pathogenesis of septic shock, will be used as a standardized experimental model of systemic inflammatory response in humans. The assessment of outcome parameters will include measurements of ocular blood flow, forearm blood flow and plasma concentration of cytokines. Measurements of ocular hemodynamics provide an unique chance to investigate local blood flow in humans non-invasively. Moreover, the retina is especially susceptible to oxidative stress because of its high consumption of oxygen, its high polyunsaturated fatty acid content, and its exposure to visible light. Evidence from literature clearly supports a role for oxidative stress in pathophysiology of several ocular diseases including diabetic retinopathy and age-related macular degeneration. To investigate the retinal vascular reactivity we will use systemic hyperoxia as a stimulus. The measurement of forearm blood flow will be use to assess endothelial function. The main study objective is to investigate the effect of oral vitamins and minerals supplementation on impaired retinal vascular reactivity after LPS administration.

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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Men aged between 18 and 35 years, nonsmokers
  • Body mass index between 15th and 85th percentile
  • Normal findings in the medical history and physical examination unless the investigator considers an abnormality to be clinically irrelevant
  • Normal laboratory values unless the investigator considers an abnormality to be clinically irrelevant
  • Normal ophthalmic findings, ametropia < 3 Dpt

排除标准

  • Regular use of medication, abuse of alcoholic beverages, participation in a clinical trial in the 3 weeks preceding the study
  • Treatment in the previous 3 weeks with any drug, vitamins and minerals supplements as well
  • Symptoms of a clinically relevant illness in the 3 weeks before the first study day
  • History of hypersensitivity to the trial drug or to drugs with a similar chemical structure
  • History or presence of gastrointestinal, liver or kidney disease, or other conditions known to interfere with, distribution, metabolism or excretion of study drugs
  • Blood donation during the previous 3 weeks

研究组 & 干预措施

1

Active Comparator

干预措施: vitamin and mineral supplement (Drug)

1

Active Comparator

干预措施: Escherichia coli Endotoxin (LPS) (Drug)

1

Active Comparator

干预措施: 100% O2 (Drug)

1

Active Comparator

干预措施: nitroglycerin (Drug)

2

Placebo Comparator

干预措施: Escherichia coli Endotoxin (LPS) (Drug)

2

Placebo Comparator

干预措施: 100% O2 (Drug)

2

Placebo Comparator

干预措施: nitroglycerin (Drug)

结局指标

主要结局

Retinal blood flow

时间窗: in total 8x on 2 study days

次要结局

  • Choroidal blood flow(in total 4x on 2 study days)
  • Flow mediated dilation (FMD) of brachial artery assessed with ultrasound(in total 4x on 2 study days)
  • Blood pressure, heart rate(on 2 study days)
  • Body temperature(on 2 study days)
  • Concentration of cytokines in plasma(on 2 study days)

研究者

申办方类型
Other

研究点 (1)

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