Department of Acute Medicine, Faculty of Medical Sciences in Zabrze, Medical University of Silesia in Katowice, Poland
Zabrze, Silesian Voivodeship, 41-800, Poland
NCT Number: NCT07242027
This observational study aims to determine whether three blood test ratios - lactate-to-albumin, CRP-to-albumin, and procalcitonin-to-albumin - can predict in-hospital mortality among critically ill adults. The study includes all adult patients admitted in 2024 to the ICU Ward B at the Silesian Center for Heart Diseases (SCCS) in Zabrze. Researchers will analyze retrospective clinical and laboratory data from electronic medical records, including lab values collected at ICU admission, patient demographics, diagnoses, and outcomes. The biomarker ratios will be manually calculated in Excel and statistically evaluated. The main goal is to assess whether these ratios are associated with patient survival and to identify predictive cut-off values to support early risk stratification in the ICU setting.
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Zabrze, Silesian Voivodeship, 41-800, Poland
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 100 days from the date of ICU admission
All-cause in-hospital mortality among ICU patients during the index hospitalization.
Medical University of Silesia
Other
Lactate-to-albumin, CRP-to-albumin and Procalcitonin-to-albumin Ratios Predict Mortality in Critically Ill Adults: a Retrospective ICU Cohort Study
Acronym: LAR-CAR-PAR
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.
NCT02398981
Bleeding, Critical Illness
Shenzhen, Guangdong, China
View Trial DetailsNCT01753024
Acute Kidney Injury, Acute Renal Failure
Shanghai, Shanghai Municipality, China
View Trial DetailsNCT01973829
Bleeding, Coma
Homyel, Belarus
View Trial DetailsNCT02039297
Bleeding, Coma
Scottsdale, Arizona, United States
View Trial Details