Effect of Increased Convective Clearance by On-line Hemodiafiltration on All Cause and Cardiovascular Mortality in Chronic Hemodialysis Patients: The Dutch Convective Transport Study (CONTRAST)
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 715
- 试验地点
- 55
- 主要终点
- all cause mortality
研究概览
简要总结
The purpose of this study is to compare the effect of low flux hemodialysis with online hemodiafiltration on all cause mortality and a combination of cardiovascular morbidity and mortality in chronic hemodialysis patients.
详细描述
Today, an increasing number of patients with chronic renal failure (CRF) is treated with (on-line) hemodiafiltration (HDF). This practice is based on the assumption that the high incidence of cardiovascular (CV) disease, as observed in patients with CRF, is at least partially related to the retention of uremic toxins in the middle and large-middle molecular (MM) range. As HDF lowers these molecules more effectively than HD, it has been suggested that this treatment improves CV outcome, if compared to standard HD.
Thus far, no definite data on the effects of HDF on CV parameters and/or clinical end-points are available. Promising data include a reduction of left ventricular mass index (LVMi) after one year of treatment with acetate free bio-filtration (AFB). Furthermore, relatively high survival rates were reported in a single center non-experimental study on patients who were treated with HDF, if compared to the EDTA registry data on HD-treated patients. Yet, these data are of observational nature, with the possibility of being biased by confounding by indication.
As the accumulation of MMW substances has been implicated in increased oxidative stress and endothelial dysfunction, a reduction of these compounds might improve these derangements. In addition, cardiac dysfunction, atherosclerosis (as measured by left ventricular mass index [LVMi], carotid intima media thickness [CIMT]) and vascular stiffness (as measured by pulse wave velocity [PWV]) might be reduced during HDF, as compared to low-flux HD.
Therefore, we propose a prospective, randomized multicenter trial, comparing (on-line) HDF with HD. After a stabilization period, an expected number of 700 chronic HD patients will be randomized to either HDF or low-flux HD and followed during 1-6 years. Primary end points are all cause mortality and combined CV events and mortality. In addition, LVMi, PWV, CIMT and various parameters of oxidative stress, acute phase reaction (APR) and endothelial function will be assessed and compared between treatment groups.
This study will provide strong evidence on the efficacy of HDF compared to low flux HD on CV morbidity and mortality, which is currently lacking but urgently needed. It is highly likely that the outcome of this study will affect current clinical practice considerably, in the Netherlands as well as internationally. Moreover, the study will point towards the mechanisms underlying the effects of HDF.
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 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients treated by HD 2 or 3 times a week, for at least 2 months
- •Patients able to understand the study procedures
- •Patients willing to provide written informed consent
排除标准
- •Current age < 18 years
- •Treatment by HDF or high flux HD in the preceding 6 months
- •Severe incompliance (severe non-adherence to the dialysis procedure and accompanying prescriptions, especially frequency and duration of dialysis treatment and fluid restriction)
- •Life expectancy < 3 months due to non renal disease
- •Participation in other clinical intervention trials evaluating cardiovascular outcome
结局指标
主要结局
all cause mortality
时间窗: entire follow up (until dead or end of study, 1-7 years)
次要结局
- fatal and non-fatal cardiovascular events(entire follow up (until death or end of study, 1-7 years))
- Left ventricular mass index (LVMi), carotid IMT (intima media thickness), aortic pulse wave velocity (PWV)(first 3 years)
- laboratory markers of endothelial dysfunction, micro-inflammation, oxidative stress(first three years of follow up)
- lipid profiles, uremic toxins(first three years)
- quality of life(entire follow up (until death or end of study, 1-7 years))
- nutritional state(entire follow up (until death or end of study 1-7 years))
- anemia management(first 12 months of follow up)
- cost utility analysis(entire follow up (until death or end of study, 1-7 years))
- hospital admissions(entire follow up (until death or end of study, 1-7 years))
- blood pressure and antihypertensive medication(entire follow up (until death or end of study, 1-7 years))
- residual kidney function(entire follow up (until death or end of study, 1-7 years))
- mineral bone disease(entire follow up (until death or end of study, 1-7 years))
- parameters of treatment / treatment delivery(entire follow up (until death or end of study, 1-7 years))
