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临床试验/ACTRN12611000060943
ACTRN12611000060943已完成未知

A 12-week, randomised, double-blind, placebo controlled study of the sustained effects of ResvidaTM on circulatory function and cognition in obese adults

Professor Peter Howe0 个研究点目标入组 30 人开始时间: 2011年1月17日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
40 Years 至 75 Years(—)
性别
All

入选标准

  • Men or post-menopausal women (self reported cessation of menses for at least 12 months)
  • Age: 40-70 years.
  • Obese (BMI 30-45 kg/m2) but otherwise healthy

排除标准

  • - Supine BP above SBP 160 mmHg or DBP 100 mmHg
  • - Having cardiovascular disease, renal disease or diabetes
  • - Taking BP lowering medication
  • - Having any other medical condition or treatments (including supplements) which, in the opinion of the investigators, may influence the outcome of the study
  • - Smokers or those using nicotine replacement therapy
  • - Those unwilling to restrict food items containing high amounts of polyphenols (grape, grape juice, wine, peanuts, peanut butter, mulberries, green tea, soy and soy products)

研究者

发起方
Professor Peter Howe

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