Study identifier:D9480R00030
ClinicalTrials.gov identifier:NCT04466969
EudraCT identifier:N/A
CTIS identifier:N/A
Assessment of hyperkalemia`s illness and treatment burden in Chronic kidney disease and heart failure patients: HK Registry pilot study
Hyperkalemia
-
No
-
All
146
Observational
20 Years +
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Sept 2021 by AstraZeneca
AstraZeneca
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Overall study aim of this study is to analyse descriptive statistics of Patient-Reported Outcome(PROs) which will be used in the Hyperkalemia(HK) registry study in hyperkalemia patients with Chronic Kidney Disease(CKD) or Heart Failure(HF) to describe the practice patterns of hyperkalemia treatment in in clinical practice. Based on these assessments, this study will provide the information for the applicability of PRO measurements which will be used in the Hyperkalemia registry study to the study population, i.e. CKD and/or HF patients with hyperkalemia
Location
Location
Nagoyashi, Aichi, Japan, 457-8511
Location
Matsudoshi, Chiba, Japan, 271-0077
Location
Tsuchiurashi, Ibaraki, Japan, 300-0028
Location
Sashimagun, Ibaraki, Japan, 306-0433
Location
Iizukashi, Fukuoka, Japan, 820-8505
Arms | Assigned Interventions |
---|---|
HF Patients with HF with reduced Ejection Fraction (HFrEF) is enrolled if patients meet following criteria within 6 months: 1. Ejection Fraction ratio(EF) ≤40% 2. New York Heart Association(NYHA) class II-IV | - |
stages of CKD (stage 3b) CKD is diagnosed based on the following e Glomerular Filtration Rate (eGFR) categories: Stage 3b: 30 mL/min/1.73m2 ≤ eGFR <45 mL/min/1.73m2 | - |
Stages of CKD (stage 4) CKD is diagnosed based on the following eGFR categories: 15 mL/min/1.73m2 ≤ eGFR <30 mL/min/1.73m2 | - |
stages of CKD (stage 5) CKD is diagnosed based on the following eGFR categories: eGFR <15 mL/min/1.73m2 | - |
Treated by potassium binders Patients who have been treated by Potassium Binders | - |
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