Condition: Perioperative Myocardial Infarction · Perioperative Myocardial Injury · Sponsor: University Hospital, Basel, Switzerland
The goal of this observational prospective cohort study is to learn about the pathophysiology of perioperative myocardial infarction/injury in high-risk patients undergoing major non-cardiac surgery. Participants will: * Wear wearable device (Basler Band) for up to seven days after the operation or until hospital discharge * Provide three blood samples. A venous specimen of blood (25 mL) will be collected preoperatively and on postoperative days 1 and 2. * Be contacted to answer a questionnaire one year after the surgery.
This description comes directly from the study's public registry record.
Christian Müller, MD, Prof · +41 61 328 6549 · christian.mueller@usb.ch
Christian Puelacher, MD-PhD · +41 61 556 5830 · christian.puelacher@usb.ch
Always discuss trial participation with your own doctor first.
| University Hospital Basel | Basel, Canton of Basel-City, Switzerland | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05866874