Potassium Correction for Renin-angiotensin-aldosterone System Optimization in Chronic Kidney Disease
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 入组人数
- 44
- 试验地点
- 1
- 主要终点
- Albumin-creatinine ratio (ACR)
研究概览
简要总结
The goal of this placebo-controlled, double-blinded cross-over trial is to test whether patiromer, compared with placebo, better enables up-titration of RAAS-blocker treatment in patients with chronic kidney disease stage 3b/4.
The main questions it aims to answer are:
- Does patiromer allow uptitration of irbesartan, resulting in a significant reduction in albuminuria and blood pressure?
- Does patiromer allow uptitration of irbesartan, resulting in a significant reduction in blood pressure?
The trial contains the following interventions:
- Participants will be switched from their ACEi/ARB to a standardised dose of irbesartan (150 mg/d).
- During two 12-week study periods, participants will receive either patiromer 8.4 g/d or placebo. The order of study periods is randomized.
- At the start of each study period irbesartan will be up-titrated to 300 mg/d.
- After 1 and 6 weeks, at both periods, plasma potassium will be measured and the irbesartan dose will be reduced to 150 mg/d in case plasma potassium exceeds 5.0 mmol/L.
- At 12 weeks from the start of the study period, the endpoints will be assessed.
- Between the two study periods, there is a 6-week washout. Irbesartan dose during the wash-out period will be 150mg/d. After washout, participants will switch from the patiromer arm to the placebo arm or vice versa.
详细描述
The PROMISE trial is a randomized, double-blind, placebo controlled cross-over trial where individuals are participating for 36 weeks. The trial consists of a 6-week run-in period, followed by two 12-week study periods, separated by a 6-week washout period.
First, during a run-in period, each participant will be converted from their ACEi/ARB dose to irbesartan 150 mg once daily. Individuals who already used irbesartan 150mg once daily before trial participation will remain on this dose during the run-in period. After six weeks, blood and 24-hour urine samples will be collected (baseline visit) and participants will be randomized to patiromer or placebo (start of study period A). The participant, research team, and treating physician will be blinded to treatment allocation (patiromer or placebo), while irbesartan will remain open-label.
At one week after start of study period A and B, participants will perform a home blood pressure measurement and visit a local lab to verify the plasma potassium level (safety visit), in combination with a scheduled phone consultation. The following actions may be taken: 1) If plasma potassium is >5.0 mmol/L or eGFR is >25% lower than baseline, the dose of irbesartan will be reduced to 150 mg/d and remain so during the remainder of the study period; 2) If systolic blood pressure is <110 mmHg, the participant has symptoms of hypotension, and plasma potassium is <5.0 mmol/L, antihypertensive co-medication may be adjusted, if applicable. If there is no antihypertensive co-medication that can be adjusted, the irbesartan dose will be reduced to 150 mg/d during the remainder of the study period.
At six weeks after start of the study period, there will be an in-hospital study visit. Blood samples will be collected, and office blood pressure will be measured. Any of the same two actions as described above may be taken in case of hyperkalaemia, severe acute kidney function decline or hypotension, respectively.
At the end of each 12-week study period, blood and 24-hour urine samples will be collected, and home (as well as office) blood pressure will be measured to establish the study endpoints. In addition, the study medication (patiromer/placebo) will be stopped and irbesartan dose will be reduced (or maintained) at 150 mg once daily. After a 6-week washout period, the second baseline will take place (measurements identical to the first baseline), which marks the start of study period B. During study period B, participants who had been randomized to patiromer in period A will now receive placebo and vice versa. The measurements during study period B will be identical to period A. At 12 weeks after the start of study period B, the protocol is completed and patients will return to their original medication.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Care Provider, Investigator)
盲法说明
Participants, care providers and investigators will be blinded regarding the use of patiromer vs. placebo during the two study periods. Irbesartan will be open label.
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
- •Age ≥ 18 years;
- •CKD stage 3b-4 (eGFR 15-44 mL/min/1.73 m2)
- •Albumin-creatinine ratio >3 mg/mmol, or proteinuria >0.05g/24u, or protein-creatinine ratio > 5mg/mmol
- •Systolic blood pressure >130 mmHg or use of one or more antihypertensive drugs;
- •Serum K+ 4.0-5.0 mmol/L;
- •On sub-maximal dose ACEi/ARB
排除标准
- •prior ACEi/ARB dose reduction due to a drop in eGFR by >25% in the last year;
- •history of severe hyperkalaemia (>6.0 mmol/L) in the last year;
- •pregnancy or breastfeeding
- •life expectancy <12 months
- •the use of lithium, potassium-sparing diuretics, potassium supplements, trimethoprim or NSAIDS
- •kidney transplant recipients, or diagnosis of autosomal dominant polycystic kidney disease or other non-glomerular kidney disease
研究组 & 干预措施
Patiromer
All participants will receive patiromer 8.4g/d (powder for oral suspension) during one of the two 12-week study periods. Following a 6-week washout, participants will switch from the patiromer arm to the placebo arm or vice versa (cross-over design).
干预措施: Patiromer 8400 MG [Veltassa] (Drug)
Placebo
All participants will receive placebo 8.4g/d (powder for oral suspension) during one of the two 12-week study periods. Following a 6-week washout, participants will switch from the patiromer arm to the placebo arm or vice versa (cross-over design).
干预措施: Placebo (Drug)
结局指标
主要结局
Albumin-creatinine ratio (ACR)
时间窗: At the end of both 12-week study periods (patiromer and placebo)
The primary study endpoint is the difference in ACR in 24-hour urine at the end of each study visit, compared to the ACR at the start of the study period. This is a continuous variable that will be presented quantitatively. In case of non-normal distribution, this parameter will be log-transformed. The primary hypothesis test will be the difference between placebo and treatment groups after 2 periods.
次要结局
- Kidney function(At the end of both 12-week study periods (patiromer and placebo))
- Blood pressure(At the end of both 12-week study periods (patiromer and placebo))
- Plasma potassium(At the end of both 12-week study periods (patiromer and placebo))
- Adverse events(At the end of both 12-week study periods (patiromer and placebo))
- Irbesartan dose(At the end of both 12-week study periods (patiromer and placebo))