A Clinical Trial to Define the Best Strategy for the Management of Heart Failure in Elderly Patients
- Conditions
- Heart FailureChronic Kidney Diseases
- Interventions
- Drug: Standard of care treatment (RAASi therapy)
- Registration Number
- NCT06578078
- Lead Sponsor
- Fundación para la Investigación del Hospital Clínico de Valencia
- Brief Summary
Heart failure (HF) and Chronic Kidney Disease (CKD) patients are frequently not administered renin-angiotensin aldosterone system inhibitor (RAASi) therapies at recommended doses due to hyperkalaemia, despite proven mortality and morbidity benefits. Sodium zirconium cyclosilicate (SZC) is a nonabsorbed potassium binder proven to lower serum potassium (S-K) and maintain normokalaemia. The purpose is to assess if a treatment regimen containing SZC will allow RAASi therapies to be optimized to target doses in patients with heart failure, chronic kidney disease and elevated serum potassium or at risk of developing elevated serum potassium.
- Detailed Description
This is a randomized clinical trial, multicentre, parallel group, open label, to evaluate the use of sodium zirconium cyclosilicate (SZC) to optimize RAASi therapy in patients with heart failure and chronic kidney disease, through up-titration of ACEi, ARB, ARNI or MRA therapy according to clinical guidelines (1), without inducing clinically significant hyperkalemia. Eligible subjects will have been admitted to hospital because of an HF (NYHA I- III) decompensation, will have required intravenous diuretics and will have had mild hyperkalaemic values that needed stabilization or be at risk of developing hyperkalaemia. Subjects will be randomised in a 1:1 ratio to receive SZC or none (standard of care treatment without potassium binders) for 3 months while optimizing RAASi therapies according to the European Society of Cardiology (ESC) guidelines.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 94
- Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.
- Provision of informed consent form prior to any study specific procedures, sampling and analysis.
- Individuals must be ≥ 70 years of age at the time of signing the informed consent form.
- Individuals must have a confirmed diagnosis of Heart Failure (HF) according to clinical practice guidelines NYHA functional class I-III (with HFrEF or HFpEF).
- Individuals must have previously been admitted to hospital due to HF decompensation requiring intravenous diuretics.
- Individuals must have been stabilised for at least 24-48h of their HF decompensation before randomisation.
- Individuals must have a confirmed diagnosis of Chronic Kidney Disease defined as a renal impairment of eGFR less than 60ml/min/1.73 m2.
- Individuals receiving background standard of care for HF and treated according to international guidelines. Specific treatment should include RAASi and/or MRA treatment and at least should have been stable for ≥ 4 weeks at maximum tolerated doses.
- Patients on RAASi blocker treatment with less than or equal to 75% of the maximum recommended dose.
- Hyperkalemic patients (sK+ 5.1-5.9 mmol/L at screening / study enrolment) or Normokalemic patients at risk of developing HK defining as having a history of hyperkalaemia (sK+ >5.0 mEq/L) within the prior 24 months and sK+ ≥4.5 mEq/L ≤ 5.1 mEq/L at inclusion
- Limited life expectancy (less than 1 year) according to clinician's criteria, such as but not limited to malignancy, with life expectancy of less than 2 years based on investigator's clinical judgement.
- sK >6 mEq/litre or <4.5mEq/litre or history of hypokalemic episodes (S-K<3.5 mEq/L) during the last year.
- Patients on haemodialysis or haemofiltration
- NYHA functional class IV
- Patients undergoing treatment with potassium binders.
- Active tumour undergoing chemotherapy or metastasis or malignancy requiring treatment.
- Symptomatic or uncontrolled atrial fibrillation despite treatment, or asymptomatic sustained ventricular tachycardia. Subjects with atrial fibrillation controlled by medication are permitted.
- QTc(f) > 550 msec.
- History of QT prolongation associated with other medications that required discontinuation of that medication.
- Congenital long QT syndrome.
- Prior history of hypersensitivity to a RAAS blocker drug, including but not limited to development of angioedema, icterus, hepatitis, or neutropenia or thrombocytopenia requiring treatment modification. Addison's disease or other causes of hypoaldosteronism.
- Patients with a known hypersensitivity to SZC or any of the excipients of the product.
- Individuals treated with potassium binding resins such as sodium polystyrene sulfonate (SPS, e.g. Kayexalate®) or calcium polystyrene sulfonate (CPS; e.g. Resonium®) or the cation exchange polymer, patiromer sorbitex calcium (Veltassa®) within 7 days prior to the first dose of study drug.
- Treated with potassium supplements within 7 days prior to randomization. 15. Positive hepatitis C antibody hepatitis B virus surface antigen or hepatitis B virus core antibody, at screening.
- Known to have tested positive for human immunodeficiency virus.
- Known history of drug or alcohol abuse within 3 year of screening.
- Involvement in the planning and/or conduct of the study (applies to both Investigator staff and/or staff at the study site).
- Judgment by the investigator that the subject should not participate in the study if the subject is unlikely to comply with study procedures, restrictions and requirements.
- Previous enrolment in the present study.
- Participation in another clinical study with an investigational product during the last 3 months.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description SZC group Sodium Zirconium Cyclosilicate Sodium zirconium cyclosilicate with standard of care treatment (RAASi therapy) Control group Standard of care treatment (RAASi therapy) Standard of care treatment (RAASi therapy) without Sodium zirconium cyclosilicate
- Primary Outcome Measures
Name Time Method Number of patients increasing at least 25% of the target doses of RAASi since the screening visit (V0) to 3 months after study inclusion (V9) Through study completion, an average of 3 months To compare the number of patients achieving an increase of at least 25% of RAASi according to guideline-recommended target doses, in the arm treated with Lokelma plus RAASi versus the arm treated with RAASi without K+ binder, at 3 months after study inclusion.
- Secondary Outcome Measures
Name Time Method Number of patients achieving at least 50% of the target doses of RAASi since the screening visit (V0) to 3 months after study inclusion (V9) Through study completion, an average of 3 months To assess the number of patients achieving at least 50% of the target dose of RAASi recommended in the guidelines.
Number of patients increasing 50% of RAASi doses since the screening visit (V0) to 3 months after study inclusion (V9) Through study completion, an average of 3 months To assess the number of patients achieving at least 50% of the target dose of RAASi recommended in the guidelines.
Trial Locations
- Locations (6)
Hospital Universitario Fundación Alcorcón
🇪🇸Alcorcón, Madrid, Spain
Hospital Universitario Severo Ochoa
🇪🇸Leganés, Madrid, Spain
Hospital Universitario Nuestra Señora del Perpétuo Socorro
🇪🇸Albacete, Spain
Hospital Universitario de Burgos
🇪🇸Burgos, Spain
Hospital Universitario Reina Sofía
🇪🇸Córdoba, Spain
Hospital Clínico Universitario de Valencia
🇪🇸Valencia, Spain