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临床试验/NCT03424317
NCT03424317终止不适用

Evaluation of the Therapeutic Effect of Sodium Intake Reduction by Education in Patients With Treatment Resistant Hypertension

DongGuk University2 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2018年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
5
试验地点
2
主要终点
Difference of change of sitting systolic blood pressure

研究概览

简要总结

The aim of this study was to evaluate the therapeutic effect of sodium intake reduction by education in patients with resistant hypertension.

The study was designed to maximize the compliance to antihypertensive agents and use optimal doses of antihypertensive agents including diuretics for 2 months before randomization. Patients will be assigned randomly to receiving (1) education of sodium intake reduction and exercise, or (2) education of exercise alone. Education of sodium intake reduction will be blinded to patients, and education of exercise will be provided to both group to blind the subjects. Daytime ambulatory blood pressure is adopted for diagnosis of resistant hypertension to avoid white-coat effect.

详细描述

The study consists of 3 phases. The first phase is to exclude pseudo-resistant hypertension by improving compliance to antihypertensive medications. Patients should visit with a prescribed antihypertensive drugs to calculate compliance to medication. If patient has compliance to medication >= 85% [= (the number of pills dispensed - the number of pills counted) / the number of pills expected to have been taken (calculated by multiplying the daily dose by the number of days since the date dispensed)], ambulatory blood pressure will be measured.

If the patient had compliance to medication >= 85%, and daytime ambulatory blood pressure >=135/85 mmHg, he will be entered into first phase of treatment. If patient had compliance to medication <85%, patients will be asked to enhance medication adherence to 85% or more, and revisit after 1 months.

In the first phase of treatment, dose of current antihypertensive medications (diuretics should be included) will be escalated to optimal doses. Three or more classes of antihypertensive drugs should be prescribed, and educate to keep compliance to medication >=85%. The duration of second phase of treatment is 2 months. After start of first phase, there is a monitoring visit monitoring of adverse drug reaction of diuretics for safety. If there is adverse drug reaction, the dose of suspected drug will be decreased. After 2 months of treatment, if daytime ambulatory blood pressure is >= 135/85 mmHg with compliance to medication >=85%, the patients will be entered into second phase of treatment.

In the second phase of treatment, patients will be randomly assigned to receive either education of exercise or education of exercise and low sodium diet (intensive education with education materials). To the patients assigned to exercise education, detailed training of diet control using educational materials will not be provided. The patients will be blinded to educational group assignments. The duration of second phase of treatment is 1 month. Before start and after completion of second phase of treatment, the amount of sodium intake will be measured by 24-hour urine sodium excretion.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

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

入选标准

  • individuals who agreed to participate in the study and submitted written informed consent
  • individuals aged 20 or more years
  • Hypertensive patients whose blood pressure is not controlled normally while taking three or more antihypertensive agents including diuretics
  • Diuretics should be Hydrochlorothiazide or Indapamide

排除标准

  • Systolic blood pressure ≥ 220 mmHg
  • Chronic kidney disease: estimated Glomerular filtration rate by Modification of Diet in Renal Disease formula ≤ 30 mL/min
  • Hyperkalemia (>5.5 mmol/L) or hypokalemia (<3.5 mmol/L)
  • Hyponatremia (<135 mmol/L)
  • Major cardiovascular events (MI, unstable angina, coronary revascularization, stroke) within 6 month of screening
  • Retinal bleeding within 3 months
  • Heart failure stage 3 or 4
  • Severe liver disease
  • Pregnancy or women in the fertile age not using efficient contraceptive methods
  • Alcoholism
  • Renovascular disease

结局指标

主要结局

Difference of change of sitting systolic blood pressure

时间窗: from randomization to completion of second phase of treatment (sodium intake reduction phase, for 1 month)

Comparison of the difference of sitting systolic blood pressure after completion of second phase of treatment (sodium intake reduction phase) from randomization of Second phase of treatment between groups

次要结局

  • Effect of sodium intake reduction(from randomization to completion of second phase of treatment (sodium intake reduction phase, for 1 month))
  • Comparison of Percent of responders at the end of first phase treatment between groups(at the end of second phase of treatment (sodium intake reduction phase, for 1 month))
  • Effect of optimized antihypertensive treatment(From the start to the end of First phase of treatment (for 2 months))

研究者

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

Moo-Yong Rhee

Proffessor

DongGuk University

研究点 (2)

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