跳至主要内容
临床试验/NCT01928134
NCT01928134已完成不适用

The Efficacy of Vitamin K2 on Human Osteoporosis, Blood-vessel Calcification and Sclerosis

Changhua Christian Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2011年4月1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
60
试验地点
1
主要终点
Change from baseline in Serum Calcium

研究概览

简要总结

This study used the generally recognized as safe (GRAS) grade of Bacillus subtilis natto to produce Vitamin K2, Menaquinone-7(MK-7), via fermentation, for functional evaluation. There are four major objectives for this study: (1) bioavailability of calcium; (2) evaluation of bone density improvement; (3) evaluation of blood-vessel calcification and sclerosis improvement; (4) safety evaluation.

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
Double (Participant, Investigator)

入排标准

年龄范围
20 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Men and non-pregnant women who are at least 20 years and under 75 years of age; and
  • •Female subjects cannot be pregnant or breast feeding.
  • •Patients who are, in the opinion of the Investigator, able to comply with the requirements of the study; and
  • •Patients who have been adequately informed of the nature and risks of the study and who have given written informed consent prior to receiving study medication.

排除标准

  • •Women who are pregnant, as determined by a urine pregnancy test, or breast-feeding.
  • •Presence or history of congestive heart failure (NYHA class III/IV) within the prior 12 weeks.
  • •Recent myocardial infarction (within the prior 12 weeks).
  • •Unstable angina pectoris.
  • •Known or suspected renal insufficiency defined as creatinine>1.5mg/dl.
  • •Known or suspected hepatic insufficiency defined as abnormal liver function tests (GOT/GPT) >3x upper normal limit (i.e., 120 U/l).
  • •Known hypomotility syndrome: (such as hypothyroidism or scleroderma).
  • •Recent major trauma within the prior 12 weeks.
  • •Recent surgery requiring anesthesia including coronary artery bypass graft (within 12 weeks).
  • •Recent hospitalization (within 12 weeks)
  • •Uncontrolled hypertension (defined as a systolic blood pressure>180mmHg or a diastolic blood pressure >105mmHg).
  • •Uncontrolled hyperlipidemia (defined as total cholesterol>240mg/dL or triglyceride >200mg/dL).
  • •Uncontrolled diabetes (defined as HbA1c>7%).
  • •Cigarette smoker (>=1/day).
  • •Acute infection requiring current antibiotic therapy.
  • •Current use of anticoagulant medication (e.g., warfarin).
  • •Recent or abrupt change (within 1 month) in usual diet.
  • •Use of an investigational drug (within 30 days prior to enrollment).
  • •Known allergies to the component of study medication
  • •Patients have acute disease, and in the opinion of investigators, are not suitable to participate in this study.

研究组 & 干预措施

A

Experimental

Vit K2+ Vit D3+ calcium carbonate (CaCO3)

干预措施: Vit K2+ Vit D3+ calcium carbonate (CaCO3) (Dietary Supplement)

B

Active Comparator

Vit K2+CaCO3

干预措施: Vit K2+CaCO3 (Dietary Supplement)

结局指标

主要结局

Change from baseline in Serum Calcium

时间窗: at 4 hours after intake

次要结局

  • Change from baseline in urine calcium/creatinine ratio(at 4 hours after intake)

研究者

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

Shih-Li Su

Attending Physician of Section of Endocrinology and Metabolism

Changhua Christian Hospital

研究点 (1)

Loading locations...

相似试验