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Clinical Trial Summary

This is a prospective study in patients who undergo routine postoperative troponin assessment after major (semi-)elective noncardiac surgery. Two groups are created based on postoperative troponin levels: Postoperative myocardial injury (PMI) group with troponin I levels ≥ 60 ng/L and a control group with troponin levels < 60ng/L. The primary aim of this study is to assess the association of PMI with pulmonary embolism. Additionally, the association between PMI and obstructive CAD will be investigated.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02682966
Study type Observational
Source UMC Utrecht
Contact
Status Enrolling by invitation
Phase N/A
Start date September 2016
Completion date December 2020