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Evaluating the effects of sevelamer carbonate on cardiovascular structure and function in chronic renal impairment in Birmingham: the CRIB-PHOS randomised controlled trial

机译:评价碳酸司维拉姆对伯明翰慢性肾功能不全患者心血管结构和功能的影响:CRIB-PHOS随机对照试验

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Background Serum phosphate is an independent predictor of cardiovascular morbidity and mortality in patients with chronic kidney disease and the general population. There is accumulating evidence that phosphate promotes arterial stiffening through structural vascular alterations such as medial calcification, which are already apparent in the early stages of chronic kidney disease. Aim To determine the effects of phosphate binding with sevelamer carbonate on left ventricular mass and function together with arterial stiffness in patients with stage 3 chronic kidney disease. Methods/Design A single-centre, prospective, randomised, double-blind, placebo-controlled trial of 120 subjects with stage 3 chronic kidney disease recruited from University Hospitals Birmingham NHS Foundation Trust. Baseline investigations include transthoracic echocardiography and cardiac magnetic resonance imaging to assess ventricular mass, volumes and function, applanation tonometry to determine pulse wave velocity and pulse wave analysis as surrogate measures of arterial stiffness and dual energy x-ray absorptiometry scanning to determine bone density. During an open-label run in phase, subjects will receive 1600 mg sevelamer carbonate with meals for four weeks. They will then be randomised to either continue sevelamer carbonate or receive an identical placebo (60 subjects per arm) for the remaining 36 weeks. Four-weekly monitoring of serum electrolytes and bone biochemistry will be performed. All baseline investigations will be repeated at the end of the treatment period. The primary endpoint of the study is a reduction in left ventricular mass after 40 weeks of treatment. Secondary endpoints are: i) change in aortic compliance; ii) change in arterial stiffness; iii) change in arterial elastance; iv) change in left ventricular systolic and diastolic elastance; v) change in left ventricular function; and vi) change in bone density. Trial Registration This trial is registered at ClinicalTrials.gov: NCT00806481 and Current Controlled Trials: ISRCTN35254279 .
机译:背景技术血清磷酸盐是慢性肾脏病患者和一般人群心血管疾病发病率和死亡率的独立预测因子。越来越多的证据表明,磷酸盐通过结构性血管改变(如内侧钙化)促进动脉硬化,这在慢性肾脏疾病的早期阶段就已经很明显了。目的确定磷酸酯与司维拉姆碳酸盐的结合对3期慢性肾脏病患者左心室质量和功能以及动脉僵硬度的影响。方法/设计从伯明翰大学NHS基金会信托基金招募的120名患有3期慢性肾脏疾病的受试者的单中心,前瞻性,随机,双盲,安慰剂对照试验。基线研究包括经胸超声心动图和心脏磁共振成像以评估心室质量,体积和功能,压平眼压测定法确定脉搏波速度和脉搏波分析以作为动脉僵硬度的替代量度,并采用双能X线吸收法扫描确定骨密度。在开放标签的分阶段试验中,受试者将在四周的饮食中接受1600毫克的司维拉姆碳酸盐。然后将他们随机分组,以继续服用司维拉姆碳酸酯或在剩下的36周内接受相同的安慰剂(每组60名受试者)。每周进行四次血清电解质和骨生物化学监测。所有基线研究将在治疗期结束时重复进行。该研究的主要终点是治疗40周后左心室重量减少。次要终点是:i)主动脉顺应性改变; ii)动脉僵硬度的变化; iii)动脉弹性变化; iv)左心室收缩和舒张弹性的改变; v)左心室功能改变; vi)骨密度变化。试验注册该试验在ClinicalTrials.gov:NCT00806481和当前对照试验:ISRCTN35254279上注册。

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