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临床试验/NCT02684643
NCT02684643已完成不适用

Study of Individualized Therapy on Hyperphosphatemia in Maintenance Hemodialysis Patients

Huashan Hospital1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2016年1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
72
试验地点
1
主要终点
Serum phosphate level at the end of the trial

研究概览

简要总结

This study is designed to study and compare the efficacy and cost-effectiveness of individualized phosphate-lowering therapy in comparison with regular guideline-recommended therapy.

详细描述

Hyperphosphatemia in hemodialysis patients has been one of the most difficult conundrums for nephrologist for the past two decades. Elevated phosphate contributes to secondary hyperparathyroidism, elevated FGF23 levels, and vascular calcification, which in turn predispose to mortality in this population. Current guidelines recommend limiting dietary phosphate intake, strengthening dialysis and using phosphate binders as three therapies for treatment of hyperphosphatemia. Yet exact clinical implication remains ambiguous: how intense restricted phosphate intake should be and how dosage of phosphate binders and dialysis should be adjusted accordingly. Thus, treatments of hyperphosphatemia have not been effective enough, but appear to be refractory. In the current study, the investigators designed individualized phosphate-lowering therapy based on each patient's phosphate-clearing ability, in order to observe and compare the efficacy and cost-effectiveness of the individualized therapy and the regular guideline-recommended therapy.

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
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •aged 18-70 years' old
  • •dialysis vintage more than 3 months on maintenance hemodialysis patients
  • •using internal arteriovenous fistula
  • •S[P] > 1.45 mmol/l, PTH (parathyroid hormone, PTH) < 900 ng/ml
  • •no residual renal function (RRF)
  • •stable dietary habit
  • •clear consciousness and capable of communication
  • •willingness to give written consent and comply with the study protocol

排除标准

  • •severe infection, anemia (Hb < 60 g/L), hypoproteinemia (Alb < 30 g/L)
  • •pregnancy, lactating women
  • •history of severe coexisting diseases such as, but not limited to, chronic liver disease, myocardial infection, cerebrovascular accident, malignant hypertension
  • •history of malignancy
  • •participation in other dietary, drug-related, or any other clinical trials within 1 month
  • •history of complications related to elevated S[P] such as, but not limited to primary hypoparathyroidism, type II vitamin D dependent rickets
  • •history of non-compliance
  • •intolerance to the individualized therapy
  • •in use of calcitonin and diphosphonate

研究组 & 干预措施

enhanced individualised therapy

Experimental

Patients' dialysis dosage, medication as well as dietary plan will be modified.

干预措施: enhanced individualised therapy (Other)

non-enhanced individualised therapy

Experimental

Patients' medication as well as dietary plan will be modified without alteration of dialysis dosage.

干预措施: non-enhanced individualised therapy (Other)

regular intervention

Experimental

Phosphate binders and calcitriol will be prescribed and adjusted without altering patients' diet habit.

干预措施: regular intervention (Other)

结局指标

主要结局

Serum phosphate level at the end of the trial

时间窗: 6 weeks

次要结局

  • cost of the therapy(6 weeks)
  • Serum calcium(6 weeks)
  • parathyroid hormone(6 weeks)

研究者

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

Chen Jing

Chief Physician of Division of Nephrology, Professor, Associate Director of Division of Nephrology and Director of Dialysis Centre

Huashan Hospital

研究点 (1)

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