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临床试验/NCT01255020
NCT01255020已完成不适用

Safety and Efficacy Evaluation of Restricted Protein Dietary Supplemented With α-keto Acid on Protecting Residual Renal Function in CAPD Patients--A Prospective, Double Blind Randomized, Parallel Control, Multi-center Clinical Trial

Sun Yat-sen University1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2010年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
160
试验地点
1
主要终点
The longitudinal change in residual glomerular filtration rate (GFR)

研究概览

简要总结

The prospective, double blind randomized, parallel control, and multi-center clinical trial will evaluate the safety and efficacy of α-keto acid with restricted protein diet on protecting residual renal function in continuous ambulatory peritoneal dialysis (CAPD) patients.

详细描述

Residual renal function (RRF) is associated with cardiovascular complication, nutritional status, incidence of peritonitis, and quality of life in peritoneal dialysis (PD) patients. Therefore, RRF is an important determinant of mortality and morbidity in PD patients.

Previous studies have suggested that dietary protein restriction supplemented with α-keto acids may slow the loss of RRF in chronic kidney disease patients. However, these trials are small sample and short-time research. In PD patients, there is very few reports to indicate the effect of α-keto acid with restricted protein diet on RRF.

The aim of this study is to evaluate the safety and efficacy of α-keto acid with restricted protein diet on protecting residual renal function in continuous ambulatory peritoneal dialysis (CAPD) patients.This is a prospective, double blind randomized, parallel control, and multi-center clinical study. 160 patients who meet Inclusion/Exclusion criteria will be randomized into α-Keto Acid group or control group at the ratio of 1:1. The α-Keto Acid group will use compound α-Keto Acid plus restricted protein diet, while control group will use placebo plus restricted protein diet.The α-Keto Acid dosage is 100mg/kg/d daily. The restricted protein dosage is 1g/kg/d. The safety and efficacy of α-Keto Acid with restricted protein diet on RRF will be evaluated after 1 year treatment.

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
Triple (Participant, Investigator, Outcomes Assessor)

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

入选标准

  • Patients on peritoneal dialysis (PD) at least three month prior to study entry.
  • Subjects of either sex, more than 18 years old, the range of age is 18 to 70 year old.
  • Residual GFR ≥ 3 ml/min/1.73m
  • Without α-Keto Acid therapy in recent 4 weeks.
  • Subjects who agree to participate in the study and sign the informed consent.

排除标准

  • History of peritonitis or other infection within one month.
  • Patients with insufficient dialysis.
  • History of taking drug which may influence amino acid metabolism within one month(glucocorticoid, thyroxin, antithyroid drug, androgens,amino acids,et al).
  • Patients with diseases which contraindicate ketosteril.
  • Cannot control diet according to protocol.
  • Alcohol abuse or drug abuse.
  • Having malignant tumor.
  • History of psychiatric or neuropathic dysfunction.
  • Cardiac failure, with New York Heart Association (NYHA) grade III-IV or history of severe heart and cerebrovascular disease in recent one month(acute stroke, acute heart failure, Lability angina)
  • Serum albumin < 30g/l.
  • Serum calcium > 2.8mmol/l.
  • Participation in another clinic trial within last three months

研究组 & 干预措施

α-Keto Acid plus restricted protein diet

Active Comparator

Participants randomized to this group will receive 12 months treatment of α-Keto Acid. The dose of α-Keto Acid is 100mg/kg per day and will divided into three times per day, and the α-Keto Acid will be asked to be taken during the meal. In addition, the participants will be asked to restrict the protein intake. The protein intake is restricted as 1g/kg/d.

干预措施: α-Keto Acid with restricted protein diet (Drug)

Placebo plus restricted protein diet

Placebo Comparator

All participants will receive 12 months treatment of placebo, at the same time they will be asked to restrict the protein intake.The dose of placebo is 100mg/kg per day, and the protein intake is restricted as 1g/kg/d.

干预措施: Placebo plus restricted protein diet (Drug)

结局指标

主要结局

The longitudinal change in residual glomerular filtration rate (GFR)

时间窗: Every 3 months up to 12 months

次要结局

  • Nutritional status(Every 3 months up to 12 months)
  • Hospitalization(Every 3 months up to 12 months)
  • Peritoneal membrane transport characteristics(Every 3 months up to 12 months)
  • Cardiovascular events(Every 3 months up to 12 months)

研究者

发起方
Sun Yat-sen University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Xue Qing Yu

Professor

Sun Yat-sen University

研究点 (1)

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