跳至主要内容
临床试验/NCT00145756
NCT00145756已完成不适用

China Salt Substitute Study-A Randomised Trial to Determine the Long-Term Effects of a Low Sodium, High Potassium Salt Substitute on Blood Pressure Among High-Risk Individuals in Northern China

The George Institute6 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2004年5月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
600
试验地点
6
主要终点
Clinical blood pressure

研究概览

简要总结

Cardiovascular disease is a leading cause of death and disability worldwide, and blood pressure is a leading determinant of this risk. To date, strategies for blood pressure lowering have focused on drug treatment but dietary interventions such as reducing sodium intake and increasing potassium intake may also be effective. Such interventions may be particularly suitable for low- and middle-income countries in which significant dietary changes may be more easily achieved. This study will test the effect of a salt substitute on blood pressure, among individuals at high-risk from cardiovascular disease in Northern China.

详细描述

This randomised trial will clearly identify whether a low-sodium, high-potassium salt-substitute is a feasible means of lowering blood pressure in high-risk individuals in rural China. The randomised design and the large size (n=600) will ensure that the results are reliable and precise. The 12-month duration will address the long-term practicability of the intervention strategy. The study is being conducted because salt-substitute-based blood pressure lowering may be particularly appropriate for rural populations in low- and middle-income countries. First, sodium intake is often very high. Second, the salt-substitute can be easily incorporated into the diet because most food is prepared and eaten at home. Third, the intervention can be provided at very low cost.

Comparisions: Low sodium high potassium salt (65% sodium chloride, 25% potassium chloride, 10% magnesium sulphate) compared to normal salt (100% sodium chloride).

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

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Participant inclusion will be based upon the presence of:
  • •A doctor-confirmed high risk of future vascular disease defined as a history of any one of:
  • •Stroke or transient ischaemic attack
  • •Hospitalisation for management of any acute coronary syndrome
  • •Surgery or angioplasty for peripheral vascular disease
  • •Treated diabetes and age 55 years or older
  • •Systolic blood pressure >160mmHg
  • •Estimated daily sodium intake of 260mmol/24hrs (about 15g/24hrs of NaCl) or above and expectation that at least 50% of daily dietary salt intake can be replaced with the salt-substitute. This will be estimated through interview of the potential participant and the individual responsible for daily food preparation (if this is not the patient) using a structured questionnaire.
  • •Provision of informed consent

排除标准

  • •Potential participants will be excluded if:
  • •they are on potassium-sparing medication
  • •there is an established history of significant renal impairment that would preclude the use of the salt-substitute in the opinion of the responsible physician.
  • •there is any reason why either the salt-substitute or normal salt are definitely indicated or definitely contra-indicated.

结局指标

主要结局

Clinical blood pressure

次要结局

  • Food taste
  • Preferred level of saltiness
  • Spot urine sodium and potassium levels

研究者

申办方类型
Other

研究点 (6)

Loading locations...

相似试验