HyperkalaemiaVITALIZENCT06635499
VITALIZE.Use and Effectiveness of Sodium Zirconium Cyclosilicate (LokelmaTM) in the Real-world Setting in Spain
An observational study of Hyperkalaemia, run by AstraZeneca at 14 sites in Spain.
Trial summary
Primary Objective(s) \& Hypothesis(es) 1. To describe the status of kalaemia in patients treated with SZC in the real-world setting at first visit after treatment initiation. 2. To describe the usual HK management after treatment initiation with SZC in the real-world setting. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Hyperkalaemia
- How many people
- 232 participants
- Where
- 14 sitesSpain
- Study dates
- 13 Nov 2024to 20 May 2025
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: This study targets enrolment of approximately 230 patients diagnosed with hyperkalaemia who have been treated with LokelmaTM following SmPC from May 2021 up to 3 months before the start of data collection per each site in Spain. It is expected to include 20 Spanish public hospitals. Initially, each site will aim to include 10-12 patients; however, the study may turn into competitive if needed to meet the planned timelines.
Who may be able to join
- Patient of 18 years of age or older at the time of index date (*).
- Patient with a diagnosis of hyperkalaemia and/or serum potassium concentration ≥ 5 mmol/L recorded at or before the index date (*).
- Patients with an estimated glomerular filtration rate (eGFR) less than 45 ml/min/1,73m2 recorded before the index date (*).
- Patient who has initiated LokelmaTM from May 2021 until 3 months before the start data collection for each site (LokelmaTM must be used on label in accordance with Summary of Product Characteristic (SmPC)).
- Patient with a baseline measure of serum potassium levels at or within 7 days before the index date (*).
- Patients with at least one follow-up visit during the study period.
- Patient with data recorded on electronic health records ≥ 6 month before index date (*).
- () Index date: Day on which the patient starts treatment with SZC (LokelmaTM).
Who cannot join
- Patient presenting pseudohyperkalaemia
- Patients receiving renal replacement therapy
- Patient who is pregnant or breastfeeding.
- Patient who, at the time of inclusion in the study, is participating in a clinical trial that includes the use of K+ binders as an investigational medicinal product (IMP).
- Patient who has explicitly refused consent to participate in research.
- Patient medical chart is not available for data extraction or the information in it is not analyzable.
Trial locations and contacts
14 sites in 1 country.
14 sites in 1 country
Spain14 sites
Research Site
A Coruña
Research Site
Asturias
Research Site
Badajoz
Research Site
Barcelona
Research Site
Burgos
Research Site
Cadiz
Research Site
Córdoba
Research Site
Huelva
Research Site
Lleida
Research Site
Madrid
Research Site
Málaga
Research Site
Santa Cruz de Tenerife
Research Site
Valencia
Research Site
Zaragoza
About this study
Official title: A Non-interVentional, multI-center and longiTudinAL Study to Describe the Use of SodIum Zirconium CyclosilicatE (LokelmaTM) in Patients Diagnosed With Hyperkalemia in the Real-world Setting in Spain: VITALIZE Study
Primary Objective(s) \& Hypothesis(es)
- To describe the status of kalaemia in patients treated with SZC in the real-world setting at first visit after treatment initiation.
- To describe the usual HK management after treatment initiation with SZC in the real-world setting.
Read more
Secondary Objective(s) \& Hypothesis(es)
- To describe treatment patterns of patients treated with SZC in the real-world setting, as well as the SZC treatment duration.
- To describe baseline sociodemographic and clinical characteristics of patients treated with SZC in the real-world setting.
- To describe the evolution of kalaemia and other clinical parameters as well as mortality in patients treated with SZC in the real-world setting.
- To describe Healthcare Resource Utilization (HCRU) before and after SZC initiation in patients treated with SZC in the real-world setting.
- To analyse specific characteristics of use of SZC in the real-world setting according to the medical specialties.
For that purpose, a non-interventional, multicenter, longitudinal study, with secondary data collection has been designed involving 20 Spanish public hospitals ans aiming to include 230 patients (10-12 patients per site) has been designed.
Read the detailed description
Potassium metabolism disorders are among the most frequent electrolyte disturbances in clinical practice, with a spectrum of variable severity. A normal potassium level is critical for proper muscle, heart, and nerve function. An excessive level of potassium can cause abnormal heart rhythms and interfere with the functioning of skeletal muscles.
Hyperkalaemia is defined by a serum potassium concentration above the upper limit of normal: K+ ≥ 5 or 5.5 mEq/L, according to guidelines. It is considered mild when the potassium concentrations are between 5 to 5.5 mEq/L, moderate between 5.5 and 6 mEq/L, and severe if potassium concentrations are higher than 6 mEq/L. Hyperkalaemia is the most serious electrolyte disturbance because it can cause fatal ventricular arrhythmias in minutes.
In a recent meta-analysis, the pooled prevalence of hyperkalaemia (by any definition/threshold) in all adult patients was 6.3% (95%CI 5.8-6.8%) with an incidence of 2.8 cases per 100 person years, while prevalence and incidence were lower in the general population (1.3% (95%CI 1.0-1.8) and 0.4 per 100 person years, respectively). also found that the prevalence was 7.5% in non-dialysis CKD, 8.3% in diabetes, 8.0% in heart failure and 35% in dialysis-dependent CKD, demonstrating that hyperkalaemia risk is influenced by the presence or absence of underlying comorbid conditions. The incidence of hyperkalaemia also increases in the elderly population treated with drugs that induce hyperkalaemia, such as renin-angiotensin-aldosterone system inhibitors (RAASi): angiotensin-converting enzyme inhibitors (ACEi), angiotensin receptor blockers (ARBs), renin inhibitors, mineralocorticoid receptor antagonists (MRA) or potassium-sparing diuretics.
Sodium Zirconium Cyclosilicate (SZC), commercialized as LokelmaTM, is a potassium binder indicated to treat hyperkalaemia constituted by two treatment phases, an initial correction phase (10 g/3 times daily/oral), which is followed by a maintenance phase once patients reach normokalaemia (after 24-48h) (5g/once daily). LokelmaTM was approved by the European Medicines Agency (EMA) in March 2018 and was launched in Spain in Q2 2021 after having demonstrated its efficacy and safety in different populations, doses, and timelines in several clinical trials.
With the aim of giving greater support to these results and, above all, in the context of the Spanish population, complementary data are needed to understand to what extent the broad group of patients in usual clinical practice achieve normokalaemia and maintain it over the study period after initiation with LokelmaTM. The project's goal is to generate real world evidence about the use and the effectiveness of SZC (LokelmaTM) in Spain, through a retrospective Non- Interventional Study (NIS).
Primary Objective(s) \& Hypothesis(es)
- To describe the status of kalaemia in patients treated with SZC in the real-world setting at first visit after treatment initiation.
- To describe the usual HK management after treatment initiation with SZC in the real-world setting.
Secondary Objective(s) \& Hypothesis(es)
- To describe treatment patterns of patients treated with SZC in the real-world setting, as well as the SZC treatment duration.
- To describe baseline sociodemographic and clinical characteristics of patients treated with SZC in the real-world setting.
- To describe the evolution of kalaemia and other clinical parameters as well as mortality in patients treated with SZC in the real-world setting.
- To describe Healthcare Resource Utilization (HCRU) before and after SZC initiation in patients treated with SZC in the real-world setting.
- To analyse specific characteristics of use of SZC in the real-world setting according to the medical specialties.
Exploratory Objective(s) \& Hypothesis(es) 1. To describe the characteristics of the SZC responder patient according to potassium levels at first visit.
Safety Objective(s) \& Hypothesis(es)
- To describe adverse events in patients treated with SZC in the real-world setting.
- Conditions
- Hyperkalaemia
- Medical subject headings
- Hyperkalemia
What is being measured
The primary outcome is the main question the study is designed to answer.
To describe the status of kalaemia in patients treated with SZC in the real-world setting at first visit after treatment initiation.
Measured: From May 2021 up to 3 months before the start of data collection
To describe the usual HK management after treatment initiation with SZC in the real-world setting.
Measured: From May 2021 up to 3 months before the start of data collection
Secondary outcomes (5)
To describe treatment patterns of patients treated with SZC in the real-world setting, as well as the SZC treatment duration.
Measured: From May 2021 up to 3 months before the start of data collection
To describe baseline sociodemographic and clinical characteristics of patients treated with SZC in the real-world setting.
Measured: From May 2021 up to 3 months before the start of data collection
To describe the evolution of kalaemia and other clinical parameters as well as mortality in patients treated with SZC in the real-world setting.
Measured: From May 2021 up to 3 months before the start of data collection
To describe Healthcare Resource Utilization (HCRU) before and after SZC initiation in patients treated with SZC in the real-world setting.
Measured: From May 2021 up to 3 months before the start of data collection
To analyze specific characteristics of use of SZC according to the medical specialties
Measured: From May 2021 up to 3 months before the start of data collection
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Oct 2024
- Study start13 Nov 2024
- Primary completion20 May 2025
- Study completion20 May 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (5)Papers the sponsor has linked to this study.
- Other trials for HyperkalaemiaStudies of the same condition, open and under way.
- More trials run by AstraZenecaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Retrospective
- Enrolment
- 232 participants (actual)
Sponsor and investigators
- Lead sponsor
- AstraZeneca
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06635499
- Sponsor's protocol ID
- D9480R00047
- Acronym
- VITALIZE
- Status last verified
- May 2026
- First submitted
- 12 Sep 2024
- Last updated
- 22 May 2026
- Results posted
- No
- Data monitoring committee
- No
Publications
De Sequera Ortíz P, A. A. (2021). Trastornos del Potasio. Hipopotasemia. En Nefrología al día. S.l (págs. 2659-2606). Lorenzo V., López Gómez JM (Eds).
Rose BD, P. T. (2001). Hypokalemia. Clinical physiology of acid-base and electrolyte disorders. New York: McGraw-Hill.
Humphrey T, Davids MR, Chothia MY, Pecoits-Filho R, Pollock C, James G. How common is hyperkalaemia? A systematic review and meta-analysis of the prevalence and incidence of hyperkalaemia reported in observational studies. Clin Kidney J. 2021 Dec 2;15(4):727-737. doi: 10.1093/ckj/sfab243. eCollection 2022 Apr.
PubMed 35371465Larivee NL, Michaud JB, More KM, Wilson JA, Tennankore KK. Hyperkalemia: Prevalence, Predictors and Emerging Treatments. Cardiol Ther. 2023 Mar;12(1):35-63. doi: 10.1007/s40119-022-00289-z. Epub 2022 Dec 12.
PubMed 36503972Palmer BF, L. M. (1996). Effect of aging on renal function and disease. The Kidney. Philadelphia: Brenner & Rector's.
Study at a glance
From the registry record, last updated by the sponsor on 22 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Non-interVentional, multI-center and longiTudinAL Study to Describe the Use of SodIum Zirconium CyclosilicatE (LokelmaTM) in Patients Diagnosed With Hyperkalemia in the Real-world Setting in Spain: VITALIZE Study
- ClinicalTrials.gov ID
- NCT06635499
- Acronym / sponsor ID
- VITALIZE / D9480R00047
- Conditions
- Hyperkalaemia
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 232 participants (actual)
- Lead sponsor
- AstraZenecaIndustry (pharma, biotech, devices)
- Study start
- 13 Nov 2024 (actual)
- Primary completion
- 20 May 2025 (actual)
- Study completion
- 20 May 2025 (actual)
- First posted
- 10 Oct 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Primary Objective(s) \& Hypothesis(es)
- To describe the status of kalaemia in patients treated with SZC in the real-world setting at first visit after treatment initiation.
- To describe the usual HK management after treatment initiation with SZC in the real-world setting.
Secondary Objective(s) \& Hypothesis(es)
- To describe treatment patterns of patients treated with SZC in the real-world setting, as well as the SZC treatment duration.
- To describe baseline sociodemographic and clinical characteristics of patients treated with SZC in the real-world setting.
- To describe the evolution of kalaemia and other clinical parameters as well as mortality in patients treated with SZC in the real-world setting.
- To describe Healthcare Resource Utilization (HCRU) before and after SZC initiation in patients treated with SZC in the real-world setting.
- To analyse specific characteristics of use of SZC in the real-world setting according to the medical specialties.
For that purpose, a non-interventional, multicenter, longitudinal study, with secondary data collection has been designed involving 20 Spanish public hospitals ans aiming to include 230 patients (10-12 patients per site) has been designed.
Detailed description
Potassium metabolism disorders are among the most frequent electrolyte disturbances in clinical practice, with a spectrum of variable severity. A normal potassium level is critical for proper muscle, heart, and nerve function. An excessive level of potassium can cause abnormal heart rhythms and interfere with the functioning of skeletal muscles.
Hyperkalaemia is defined by a serum potassium concentration above the upper limit of normal: K+ ≥ 5 or 5.5 mEq/L, according to guidelines. It is considered mild when the potassium concentrations are between 5 to 5.5 mEq/L, moderate between 5.5 and 6 mEq/L, and severe if potassium concentrations are higher than 6 mEq/L. Hyperkalaemia is the most serious electrolyte disturbance because it can cause fatal ventricular arrhythmias in minutes.
In a recent meta-analysis, the pooled prevalence of hyperkalaemia (by any definition/threshold) in all adult patients was 6.3% (95%CI 5.8-6.8%) with an incidence of 2.8 cases per 100 person years, while prevalence and incidence were lower in the general population (1.3% (95%CI 1.0-1.8) and 0.4 per 100 person years, respectively). also found that the prevalence was 7.5% in non-dialysis CKD, 8.3% in diabetes, 8.0% in heart failure and 35% in dialysis-dependent CKD, demonstrating that hyperkalaemia risk is influenced by the presence or absence of underlying comorbid conditions. The incidence of hyperkalaemia also increases in the elderly population treated with drugs that induce hyperkalaemia, such as renin-angiotensin-aldosterone system inhibitors (RAASi): angiotensin-converting enzyme inhibitors (ACEi), angiotensin receptor blockers (ARBs), renin inhibitors, mineralocorticoid receptor antagonists (MRA) or potassium-sparing diuretics.
Sodium Zirconium Cyclosilicate (SZC), commercialized as LokelmaTM, is a potassium binder indicated to treat hyperkalaemia constituted by two treatment phases, an initial correction phase (10 g/3 times daily/oral), which is followed by a maintenance phase once patients reach normokalaemia (after 24-48h) (5g/once daily). LokelmaTM was approved by the European Medicines Agency (EMA) in March 2018 and was launched in Spain in Q2 2021 after having demonstrated its efficacy and safety in different populations, doses, and timelines in several clinical trials.
With the aim of giving greater support to these results and, above all, in the context of the Spanish population, complementary data are needed to understand to what extent the broad group of patients in usual clinical practice achieve normokalaemia and maintain it over the study period after initiation with LokelmaTM. The project's goal is to generate real world evidence about the use and the effectiveness of SZC (LokelmaTM) in Spain, through a retrospective Non- Interventional Study (NIS).
Primary Objective(s) \& Hypothesis(es)
- To describe the status of kalaemia in patients treated with SZC in the real-world setting at first visit after treatment initiation.
- To describe the usual HK management after treatment initiation with SZC in the real-world setting.
Secondary Objective(s) \& Hypothesis(es)
- To describe treatment patterns of patients treated with SZC in the real-world setting, as well as the SZC treatment duration.
- To describe baseline sociodemographic and clinical characteristics of patients treated with SZC in the real-world setting.
- To describe the evolution of kalaemia and other clinical parameters as well as mortality in patients treated with SZC in the real-world setting.
- To describe Healthcare Resource Utilization (HCRU) before and after SZC initiation in patients treated with SZC in the real-world setting.
- To analyse specific characteristics of use of SZC in the real-world setting according to the medical specialties.
Exploratory Objective(s) \& Hypothesis(es) 1. To describe the characteristics of the SZC responder patient according to potassium levels at first visit.
Safety Objective(s) \& Hypothesis(es)
- To describe adverse events in patients treated with SZC in the real-world setting.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- This study targets enrolment of approximately 230 patients diagnosed with hyperkalaemia who have been treated with LokelmaTM following SmPC from May 2021 up to 3 months before the start of data collection per each site in Spain. It is expected to include 20 Spanish public hospitals. Initially, each site will aim to include 10-12 patients; however, the study may turn into competitive if needed to meet the planned timelines.
Key inclusion criteria (8 listed)
- Patient of 18 years of age or older at the time of index date (*).
- Patient with a diagnosis of hyperkalaemia and/or serum potassium concentration ≥ 5 mmol/L recorded at or before the index date (*).
- Patients with an estimated glomerular filtration rate (eGFR) less than 45 ml/min/1,73m2 recorded before the index date (*).
- Patient who has initiated LokelmaTM from May 2021 until 3 months before the start data collection for each site (LokelmaTM must be used on label in accordance with Summary of Product Characteristic (SmPC)).
- Patient with a baseline measure of serum potassium levels at or within 7 days before the index date (*).
Key exclusion criteria (6 listed)
- Patient presenting pseudohyperkalaemia
- Patients receiving renal replacement therapy
- Patient who is pregnant or breastfeeding.
- Patient who, at the time of inclusion in the study, is participating in a clinical trial that includes the use of K+ binders as an investigational medicinal product (IMP).
- Patient who has explicitly refused consent to participate in research.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
To describe the status of kalaemia in patients treated with SZC in the real-world setting at first visit after treatment initiation.
Time frame: From May 2021 up to 3 months before the start of data collection
To describe the usual HK management after treatment initiation with SZC in the real-world setting.
Time frame: From May 2021 up to 3 months before the start of data collection
5 secondary outcomes
To describe treatment patterns of patients treated with SZC in the real-world setting, as well as the SZC treatment duration.
Time frame: From May 2021 up to 3 months before the start of data collection
To describe baseline sociodemographic and clinical characteristics of patients treated with SZC in the real-world setting.
Time frame: From May 2021 up to 3 months before the start of data collection
To describe the evolution of kalaemia and other clinical parameters as well as mortality in patients treated with SZC in the real-world setting.
Time frame: From May 2021 up to 3 months before the start of data collection
To describe Healthcare Resource Utilization (HCRU) before and after SZC initiation in patients treated with SZC in the real-world setting.
Time frame: From May 2021 up to 3 months before the start of data collection
To analyze specific characteristics of use of SZC according to the medical specialties
Time frame: From May 2021 up to 3 months before the start of data collection
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 May 2026.
- Results publicationDe Sequera Ortíz P, A. A. (2021). Trastornos del Potasio. Hipopotasemia. En Nefrología al día. S.l (págs. 2659-2606). Lorenzo V., López Gómez JM (Eds).
- Results publicationRose BD, P. T. (2001). Hypokalemia. Clinical physiology of acid-base and electrolyte disorders. New York: McGraw-Hill.
- Results publication: PubMed 35371465Humphrey T, Davids MR, Chothia MY, Pecoits-Filho R, Pollock C, James G. How common is hyperkalaemia? A systematic review and meta-analysis of the prevalence and incidence of hyperkalaemia reported in observational studies. Clin Kidney J. 2021 Dec 2;15(4):727-737. doi: 10.1093/ckj/sfab243. eCollection 2022 Apr.
- Results publication: PubMed 36503972Larivee NL, Michaud JB, More KM, Wilson JA, Tennankore KK. Hyperkalemia: Prevalence, Predictors and Emerging Treatments. Cardiol Ther. 2023 Mar;12(1):35-63. doi: 10.1007/s40119-022-00289-z. Epub 2022 Dec 12.
- Results publicationPalmer BF, L. M. (1996). Effect of aging on renal function and disease. The Kidney. Philadelphia: Brenner & Rector's.
- CSR\_VITALIZE\_19May2026\_ 1Link provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
14 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Hyperkalaemia, run by AstraZeneca at 14 sites in Spain.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 8 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 22 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 14 sites in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
To describe the status of kalaemia in patients treated with SZC in the real-world setting at first visit after treatment initiation. (time frame: From May 2021 up to 3 months before the start of data collection). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06635499, which also lists 5 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 May 2026.