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临床试验/TCTR20190205002
TCTR20190205002招募中4 期

Effects of Vitamin C, Vitamin D3, Coenzyme Q10 and antioxidant formula of different supplement forms on micronutrient, biomarker blood levels and quality of life.

A0 个研究点目标入组 72 人开始时间: 2019年2月5日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方
A
入组人数
72

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 80 Years(—)
性别
All

入选标准

  • 1.Subjects aged ≥ 18 years who visit Vital-life wellness center for micronutrient level assessment and decide to receive either Vitamin C, Vitamin D3, CO-Q10 and antioxidant formula of HCK® or The original VTL supplement of Vitamin C, Vitamin D3, CO-Q10 and antioxidant or no supplement after discussion for possible treatment options with physician as usual practice
  • 2.Subjects found to have low level of 25-(OH)D3/D2 (having 25-(OH)D3/D2 level 20-29 ng/ml) with the symptoms or feelings of low energy, lack of vitality or tiredness
  • 3.Subjects who have not taken coenzyme Q10, vitamin C, vitamin D3, vitamin E, carotenoids, and flavonoids for at least 3 months and vitamin A for at least 6 months
  • 4.Willing and able to comply with study procedure.

排除标准

  • 1.Subjects with poorly controlled underlying diseases such as poor control of Blood
  • Pressure (systolic blood pressure > 180 mmHg or diastolic blood pressure > 110 mmHg), poor control of blood sugar (HbA1c > 7%).
  • 2.Subjects with eGFR < 30 ml/min/1.73 m2
  • 3.Female subjects who are pregnant or lactating, or plan to have children (a negative
  • serum or urine pregnancy test is required on the screening day for women of child-bearing potential).
  • 4. Subjects with diseases that may interfere with supplement absorption e.g., patients
  • with malabsorption and bowel surgery.
  • 5. Subjects using medication that may interfere with micronutrient levels such as acid
  • suppressants, antacids, antiepileptic drugs (i.e., phenobarbital, valproic acid,
  • carbamazepine, phenytoin), and antipsychotic drugs (i.e., tricyclic antidepressants and
  • haloperidol). However, subjects who stop using these medications for at least 1 month
  • prior to the enrollment can be included into the study.
  • 6. Subjects with vitamin D deficiency or having underlying diseases that require
  • treatment with vitamin D such as osteoporosis and primary hyperparathyroidism
  • 7. Subjects who is currently smoking.
  • 8. Subjects with history of allergy to vitamins and supplements

研究者

发起方
A

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