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临床试验/NCT00755924
NCT00755924已完成1 期

Prospective Randomized Clinical Trial Evaluating the Impact of Vinegar on High Density Lipoprotein

HealthPartners Institute1 个研究点 分布在 1 个国家目标入组 114 人开始时间: 2008年6月1日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
114
试验地点
1
主要终点
Change in HDL-Cholesterol level

研究概览

简要总结

This is a double-blinded randomized placebo controlled prospective clinical trial evaluating the impact of apple cider vinegar on serum HDL. 112 participants will be randomized to consume either 2 tablespoons of vinegar daily or a placebo containing a 2% balsamic vinegar solution in water. Baseline, two month and 4 month blood samples will be obtained for fasting lipids. The primary endpoint is met if HDL levels increase in the treatment arm versus baseline after 2 month intervention.

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
Double (Participant, Investigator)

入排标准

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

入选标准

  • •Those older than 18 years of age
  • •Park Nicollet Health Services patient

排除标准

  • •Because of a potential positive effect of vinegar on improving diabetes mellitus8 and the subsequent change in medication regime for diabetes diabetic patients will be excluded from this study. If this study finds that vinegar does increase HDL levels, a subsequent study of diabetic patients will be conducted.
  • •History of allergy to apple cider vinegar
  • •Those with a terminal illness
  • •Diagnosis of Inflammatory bowel disease
  • •Those with Immunosuppression diseases
  • •Patients on dialysis
  • •Severe psychiatric illness who are unable to consent or reliably participate
  • •No evidence of end stage renal disease
  • •Those who use alcohol greater than or equal to 2 drinks per day
  • •Those who take in >3 tsp vinegar/day supplement
  • •Plans to increase exercise or begin diet during the protocol period
  • •Any use of niacin or niacin-like compounds
  • •Initiation of niacin, fibrates (eg gemfibrozil); statin or ezetimibe medication within the last 6 weeks or during the trial
  • •Inability to read English
  • •Age less than 18 years given clinical events would be unlikely in this population
  • •LDL greater than 160mg/dL and requires adjustment or addition of statin therapy (which could reduce HDL)
  • •History of liver failure in medical history review
  • •Current smoking (as this can reduce HDL levels and it would be unethical to require people to continue smoking during the study)

结局指标

主要结局

Change in HDL-Cholesterol level

时间窗: 12 months

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (1)

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