跳至主要内容
临床试验/NCT03672513
NCT03672513已完成不适用

Short-term Supplementation, Bone Turnover and Antioxidant Status in Postmenopausal Stage: A Placebo Controlled Study.

Universidad de Granada2 个研究点 分布在 1 个国家目标入组 78 人开始时间: 2016年9月8日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
78
试验地点
2
主要终点
Antioxidant status

研究概览

简要总结

This is a 8-week, double-blinded, placebo-controlled, randomized intervention trial to investigate the effects of Mg and Zn supplementation on antioxidant status and bone hormonal parameters. Participants were randomly assigned to one of three treatment groups: Placebo group (PbG: 25 women); Magnesium Group - 500 mg/day of Mg (MgG: 27 women); Zinc Group - 50 mg/day of Zn (ZnG: 26 women).

详细描述

Seventy-eight healthy postmenopausal volunteers aged between 44 and 76 were recruited once had been informed about the protocol. This is a 8-week, double-blinded, placebo-controlled, randomized intervention trial to investigate the effects of Mg and Zn supplementation on antioxidant status and bone hormonal parameters. Participants were randomly assigned to one of three treatment groups: Placebo group (PbG: 25 women); Magnesium Group - 500 mg/day of Mg (MgG: 27 women); Zinc Group - 50 mg/day of Zn (ZnG: 26 women).

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
None

入排标准

年龄范围
44 Years 至 76 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • to present postmenopausal status (with at least 12 months of amenorrhea)
  • to present low status in Mg and/or Zn obtained in a previous biochemical assessment
  • not present any pathology that could affect their nutritional status
  • not to be subjected to hormone replacement therapy (HRT)
  • not to demonstrate lactose intolerance
  • Exclusion criteria
  • acute or terminal illness
  • unwillingness to either complete the study requirements or to be randomised into control or experimental group
  • to be smoker
  • to be on a medication regimen

排除标准

  • 未提供

研究组 & 干预措施

Placebo Supplemented Group

Placebo Comparator

Placebo control

干预措施: Placebo Comparator (Dietary Supplement)

Magnesium Supplemented Group

Experimental

Magnesium Group

干预措施: Magnesium supplement (Dietary Supplement)

Zinc Supplemented Group

Experimental

Zinc Group

干预措施: Zinc Supplement (Dietary Supplement)

结局指标

主要结局

Antioxidant status

时间窗: 2 months

Total antioxidant capacity (TAC) determination in plasma samples was carried out evaluating the reduction power of Cu2+ from the action of antioxidants present in samples (TAC kit, Jaica, Shizuoka, Japan). Values were expressed in umol/L.

Oxidative stress

时间窗: 2 months

Glutathione peroxidase (GPx) in mU/mL and Superoxide dismutase (SOD) in U/mL. GPx activity was determined by using the Bioxytech GPx-340™ kit (OxisResearch™), an indirect colorimetric assay of the activity of c-GPx \[28\]. SOD activity was determined by using the Randox Ransod kit (RANDOX Laboratories Ltd., United Kingdom).

次要结局

  • Anthropometric assessment - Height(2 months)
  • Anthropometric assessment - Waist circumference(2 months)
  • Anthropometric assessment - Body composition by bioelectrical impedance(2 months)
  • Intake assessment(2 months)
  • Biochemical parameters - Clinical-nutritional parameters(2 months)
  • Hormonal parameters(2 months)

研究者

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

Elena Planells del Pozo

University Professor

Universidad de Granada

研究点 (2)

Loading locations...

相似试验