Clinical Trials Directory

Trials / Completed

CompletedNCT04292249

Predictive Value of suPAR and hsCRP on Postoperative Mortality in Cardiac Surgery

Predictive Value of suPAR and hsCRP on Postoperative Mortality in 951 Patients Undergoing Elective On-pump Cardiac Surgery

Status
Completed
Phase
Study type
Observational
Enrollment
951 (actual)
Sponsor
Rigshospitalet, Denmark · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study aims to investigate whether preoperative soluble urokinase plasminogen activating receptor (suPAR) and High-sensitivity C-Reactive Protein (hsCRP) are independent markers of death after cardiac surgery. Further, to assess whether suPAR and hsCRP provides increased predictive accuracy of the clinical risk model EuroSCORE II. The purpose of the study is to gain knowledge on whether these inflammatory biomarkers might be able to reveal a pro-inflammatory disease state that represents a significant risk in patients undergoing cardiovascular surgery. Hence, these biomarkers may assist clinicians in selecting compassionate treatment for high risk patients.

Conditions

Interventions

TypeNameDescription
OTHERBlood samplingAnalysis will be performed using commercially available analyses (suPARnostic® kit (validated to measure suPAR concentrations between 0.6 and 22 ng/mL) (ViroGates)). HsCRP will be measured by high sensitivity CRP assays (Tina-quant hs-CRP latex assay (validated to measure CRP concentrations between 0.3 - 20 mg/L) (Roche/Hitachi)). In patients with CRP\>20 mg/L a regular CRP-measurement will be performed.

Timeline

Start date
2012-08-06
Primary completion
2019-06-11
Completion
2019-12-16
First posted
2020-03-03
Last updated
2020-03-03

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT04292249. Inclusion in this directory is not an endorsement.