Potassium Correction for RAAS Optimization in Chronic Kidney Disease

Last updated: June 11, 2024
Sponsor: University Medical Center Groningen
Overall Status: Active - Recruiting

Phase

4

Condition

Vascular Diseases

Stress

Williams Syndrome

Treatment

Placebo

Patiromer 8400 MG [Veltassa]

Clinical Study ID

NCT06256991
17237
  • Ages > 18
  • All Genders

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age ≥ 18 years;

  • CKD stage 3b-4 (eGFR 15-44 mL/min/1.73 m2)

  • Albumin-creatinine ratio >30 mg/mmol, or proteinuria >0.5g/24u, orprotein-creatinine ratio > 50mg/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

Exclusion

Exclusion Criteria:

  • 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);

  • pregnancy or breastfeeding

  • life expectancy <12 months

  • the use of lithium, potassium-sparing diuretics, potassium supplements, trimethoprimor NSAIDS

  • kidney transplant recipients, or diagnosis of autosomal dominant polycystic kidneydisease or other non-glomerular kidney disease

Study Design

Total Participants: 50
Treatment Group(s): 2
Primary Treatment: Placebo
Phase: 4
Study Start date:
April 01, 2024
Estimated Completion Date:
December 31, 2026

Study Description

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.

The investigators chose a cross-over study design to be able to use participants as their own control; this will enhance statistical power and reduce the number of required participants. Based on previous studies, it is known that 6 weeks are sufficient to reach stable albuminuria and blood pressure after an ARB dose change. Therefore, even if halfway the 12-week study period a dose reduction is made, there is enough time for albuminuria and blood pressure to stabilize before the end of the study period (i.e., when the primary endpoint is established). A 6-week washout period is inserted to avoid carry-over effects.

Connect with a study center

  • University Medical Center Groningen

    Groningen,
    Netherlands

    Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.