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临床试验/NCT00789425
NCT00789425已完成2 期

A Randomised, Double Blind, Parallel Group, 12-month Comparison of a Standardized Olive Extract With Placebo in Postmenopausal Women With Decreased Bone Mineral Density

BioActor2 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2008年9月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
发起方
BioActor
入组人数
64
试验地点
2
主要终点
Serum levels of Osteocalcin and CTX will be used as bone turnover markers

研究概览

简要总结

The purpose of this study is to determine whether the intake of a daily dosage of standardized olive extract provides any protection against bone loss.

详细描述

Apart from estrogen deficiency, the early postmenopausal period is also characterised by an increasing inflammatory and oxidant status, which further contributes to the development of osteoporosis/osteopenia. The link between systemic inflammation and osteoporosis has only been established recently as it was found that higher circulating hsCRP levels are associated with lower bone mineral density in both healthy pre- and postmenopausal women. Furthermore, it was already known for a long time that one of the most important cytokines implicated in the pathogenesis of various metabolic bone diseases, including postmenopausal osteoporosis, is interleukin (IL)-6, which is produced by osteoblasts, monocytes and T-cells.

Olive oil is the principle fat source of the traditional Mediterranean diet, a diet that has been associated with a low incidence of some diseases, including coronary heart disease and osteoporosis. In addition to the main ingredient (ie. oleic acid) extra virgin olive oil also contains phenolic compounds, such as oleuropein- and ligstroside-aglycones and their derivatives. They are formed in olives by enzymatic removal of glucose from the polar parent compound oleuropein-glycoside. A Mediterranean diet rich in olive oil supplies 10 - 20 mg of phenols per day.

The main metabolic attribute of oleuropein is that it exerts both antioxidant and anti-inflammatory activity by lowering the levels of proinflammatory cytokines like IL-1, IL-6 or TNF-alpha. By inhibiting osteoclast activity, this may result in lowering the rate of bone resorption and, at least in part, protect against osteoporosis development.

Formulated as a capsule it is expected that the compliance and tolerability will be improved compared to the liquid administration. The present study is designed to investigate the effect of 250 mg of a standardized extract of olive polyphenols per day on bone loss in postmenopausal women with decreased bone mass (osteopenia) .

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
50 Years 至 70 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Signed written informed consent
  • Gender female
  • Between 50-70 years of age
  • At least 2 years post menopause
  • Bone mineral density (BMD) < or equal to -1.5 and > or equal to -2.5 SD% Young Adult
  • Patients with stabilised food habits
  • Patients able to understand the nature of the study and able to give signed written informed consent.

排除标准

  • Patients with any diseases affecting bone tissue e.g. primary hyperparathyroidism.
  • Patients during any therapy affecting bone tissue e.g. HRT, corticosteroids.
  • Patients with any associated illness of sufficient severity, or clinically relevant abnormalities in the pre-study screening, which in the opinion of the investigator would make them unsuitable for inclusion in the study, e.g. severe heart failure, severe ischaemic heart disease etc.
  • Planned hospitalisation (major surgery) during the study.
  • Patients who have any known allergy or intolerance to any compound in the test product.
  • Patients who are unwilling or unable to comply with the study protocol for any other reason.

研究组 & 干预措施

1

Active Comparator

a standardized extract of olive polyphenols at 250 mg per day + 1000 mg of calcium per day.

干预措施: Standardized Extract of Olive Polyphenols (Dietary Supplement)

2

Placebo Comparator

Placebo (starch) + 1000 mg of calcium per day.

干预措施: Placebo (Dietary Supplement)

结局指标

主要结局

Serum levels of Osteocalcin and CTX will be used as bone turnover markers

时间窗: 0, 3, 6, and 12 months

次要结局

  • Bone mineral density as measured by DEXA in lumbar spine and total hip(0 and 12 months)
  • hs-CRP and IL-6 in serum as inflammation markers(0, 6, and 12 months)
  • ORAC values in serum as oxidative stress marker(0, 6, and 12 months)
  • Total cholesterol, HDL-C, LDL-C, triglycerides in serum as CVD-risk markers.(0, 6, and 12 months)

研究者

发起方
BioActor
申办方类型
Industry

研究点 (2)

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