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临床试验/NCT02271230
NCT02271230已完成3 期

Intervention With Vitamin D and Omega-3 Supplements and Incident Heart Failure

Brigham and Women's Hospital1 个研究点 分布在 1 个国家目标入组 25,871 人开始时间: 2014年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
25,871
试验地点
1
主要终点
Number of Participants With New Heart Failure Hospitalization

研究概览

简要总结

This study will examine whether an intervention with vitamin D or fish oil supplements can reduce the risk of heart failure among adult men and women during a follow up period of up to five years (starting from the time of randomization into the parent VITAL trial). The investigators hypotheses are that both vitamin D and fish oil supplements will each reduce the risk of heart failure.

详细描述

For this ancillary study of the ongoing parent VITAL trial, we will adjudicate incident heart failure cases occurring during a time period of up to five years starting from randomization of subjects in the parent VITAL study. Intention-to-treat analysis will be used to assess the efficacy of vitamin D as well as omega-3 fatty acids.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Men aged 50 or older or women aged 55 or older
  • Be consuming no more than 800 IU of vitamin D from all supplemental sources combined (individual vitamin D supplements, calcium+vitamin D supplements, medications with vitamin D [e.g., Fosamax Plus D], and multivitamins), or, if taking, willing to decrease or forego such use during the trial;
  • Be consuming no more than 1200 mg/d of calcium from all supplemental sources combined, or, if taking, willing to decrease or forego such use during the trial;
  • Not be taking fish oil supplements, or, if taking, willing to forego their use during the trial

排除标准

  • prevalent heart failure
  • History of cancer (except non-melanoma skin cancer), heart attack, stroke, transient ischemic attack, angina pectoris, CABG, or PCI
  • History of renal failure or dialysis, hypercalcemia, hypo- or hyperparathyroidism, severe liver disease (cirrhosis), or sarcoidosis or other granulomatous diseases such as active chronic tuberculosis or Wegener's granulomatosis;
  • Allergy to fish or soy

研究组 & 干预措施

Vitamin D and fish oil

Experimental

2000 IU per day and 1 g per day of fish oil

干预措施: Vitamin D and fish oil (Drug)

Vitamin D alone

Placebo Comparator

2000 IU Vitamin D and fish oil placebo

干预措施: Vitamin D alone (Drug)

Fish oil (EPA/DHA) alone

Experimental

1 g per day of fish oil and vitamin D placebo

干预措施: Fish oil (EPA/DHA) alone (Dietary Supplement)

Fish oil and vitamin D placebo

Placebo Comparator

Placebo for both vitamin D and fish oil

干预措施: Placebo (Other)

结局指标

主要结局

Number of Participants With New Heart Failure Hospitalization

时间窗: 5 years

We will consider any hospitalization for heart failure among participants enrolled in the parent VITAL trial for this ancillary study. Incident heart failure are initially captured through annual questionnaires with subsequent validation by a team of physicians with expertise in cardiovascular medicine and epidemiology. We excluded 36 participants with prevalent heart failure at the time of randomization for the primary analysis.

次要结局

  • Number of Recurrent Heart Failure Hospitalization(5 years)

研究者

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

Luc Djousse

Director of Research, Associate Professor of Medicine

Brigham and Women's Hospital

研究点 (1)

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