Site SE46001
Uppsala, SE-75185, Sweden
NCT Number: NCT04042350
The purpose of this study is to evaluate which clinical and laboratory factors are associated with major adverse cardiovascular event (MACE) in chronic kidney disease (CKD) patients on dialysis.
The study will also establish a cardiovascular (CV) risk equation appropriate for this dialysis population.
Looking for future studies?
Notify Me50 year–80 year
All sexes
Observational
Uppsala, SE-75185, Sweden
This study is a retrospective analysis of dialysis dependent CKD patients participating in AURORA. The retrospective analysis will be performed using the AURORA study database.
AURORA was a prospective clinical trial in which dialysis patients were randomly assigned to rosuvastatin or placebo, sponsored by AstraZeneca. Patients included in the AURORA study who had end stage renal disease (ESRD) and had been treated with regular hemodialysis or hemofiltration for at least 3 months. Patients were recruited from approximately 300 centers in 25 countries.
The clinical study data is held by AstraZeneca AB, Sweden.
No formal sample size calculation was performed. The sample size is based on the available data from the AURORA study.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Exploring clinical risk factors associated with the risk for cardiovascular events and mortality, rather than to evaluate specific drugs.
Time frame: Up to a maximum of 5.6 years
A MACE is defined as a non-fatal myocardial infarction (MI), non-fatal stroke, and CV mortality.
Time frame: Up to a maximum of 5.6 years
CV events include non-fatal MI, unstable angina, coronary revascularization therapy, new onset heart failure, non-fatal stroke or all-cause mortality.
Time frame: Up to a maximum of 5.6 years
Time to individual CV event.
Time frame: Up to a maximum of 5.6 years
Time to individual CV event.
Time frame: Up to a maximum of 5.6 years
Time to individual CV event.
Time frame: Up to a maximum of 5.6 years
Time to individual CV event.
Time frame: Up to a maximum of 5.6 years
Time to individual CV event.
Time frame: Up to a maximum of 5.6 years
Time to death caused by a CV event.
Time frame: Up to a maximum of 5.6 years
Time to death from any cause.
Astellas Pharma Europe Ltd.
Industry
A Retrospective Analysis Assessing Clinical Risk Factors for Cardiovascular Events and Mortality and Development of a Risk Calculator in Chronic Kidney Disease Stage 5 on Dialysis Treatment Using Data From the AURORA Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07660757
Cardiovascular Diseases, Chronic Disease
Roma, Italy
View Trial DetailsNCT01530958
Chronic Disease, Chronic Kidney Disease (CKD)
San Francisco, California, United States
View Trial DetailsNCT07381101
Chronic Disease, Chronic Kidney Disease (CKD)
London, Ontario, Canada
View Trial DetailsNCT07399795
Chemically-Induced Disorders, Chronic Disease
London, Ontario, Canada
View Trial Details