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临床试验/EUCTR2012-001249-41-FR
EUCTR2012-001249-41-FR进行中(未招募)1 期

Vitamin D3 – Omega3 – Home Exercise – HeALTHy Ageing and LongevityTrial Randomized, double-blind, placebo-controlled, multi-centre clinicaltrial - DO – HEALTH

niversity Hospital of Zurich and City Hospital Waid0 个研究点目标入组 2,152 人开始时间: 2013年7月29日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
2,152

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Mini Mental State Examination Score of at least 24
  • - Living in the community
  • - Sufficiently mobile to come to the study centre, to walk 10 meters with or without walking aid and to get in and out of a chair without help
  • - Able to swallow study medication
  • - Able and willing to participate, sign informed consent (including consent to analyze all samples until withdrawal) and cooperate with study procedures
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 2152

排除标准

  • (1) Consumption of more than 1000 IU vitamin D/day in the 6 month prior to enrolment, and/or a bolus of 300'000 IU vitamin D or more in the 12 month prior to enrolment, and /or unwillingness to limit vitamin D intake to the current standard of 800 IU/day of vitamin D during the course of the trial
  • (2) Unwillingness to limit calcium supplement dose to 500 mg per day for the duration of the trial
  • (3) Taking omega-3 fat supplements and unwilling to forgo their use for the duration of the trial
  • (4) Use of any active vitamin D metabolite (i.e. Rocaltrol,
  • alphacalcidiol), PTH treatment (i.e. Teriparatide), or Calcitonin at
  • baseline and unwillingness to forego these treatments during the
  • course of the trial
  • (5) Current or recent (previous 4 months) participation in another clinical trial, or plans of such participation in the next 3 years (corresponding to DO-HEALTH length)
  • (6) Presence of the following diagnosed health conditions in the last 5 years: history of cancer (except non-melanoma skin cancer); myocardial infarction, stroke, transient ischemic attack, angina pectoris, or coronary artery intervention
  • (7) Severe renal impairment (creatinine clearance = 15 ml/min) or
  • dialysis, hypercalcaemia (> 2.6 mmol/l)
  • (8) Hemiplegia or other severe gait impairment
  • (9) History of hypo- or primary hyper-parathyroidism
  • (10) Severe liver disease
  • (11) History of granulomatous diseases (i.e. tubercolosis, sarcoidosis)
  • (12) Major visual or hearing impairment or other serious illness that would preclude participation
  • (13) Living with a partner who is enrolled in DO-HEALTH (we exclude couples)
  • (14) Living in assisted living situations or a nursing home
  • (15) Temporary exclusion: acute fracture in the last 6 weeks
  • (16) Epilepsy and/or use of anti-epileptic drugs
  • (17) Individuals who fell more than 3 times in the last month
  • (18) Osteodystrophia deformans (M. Paget, Paget's disease)

研究者

发起方
niversity Hospital of Zurich and City Hospital Waid

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