Monitoring of Vital Signs for Phenotyping of Perioperative Myocardial Infarction/Injury After Noncardiac Surgery
Recruiting now
Conditions studied: Perioperative Myocardial Infarction, Perioperative Myocardial Injury
In brief
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.
Key facts
- Study ID
- NCT05866874
- Run by
- University Hospital, Basel, Switzerland
- People needed
- 875
- Starts
- 2022-09-20
- Expected to finish
- 2026-12-01
- Last updated by the study team
- 2025-01-28
Who can join
Age: 40 and older, up to 85. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient eligible for routine PMI-screening
- Patient requiring hospitalisation with ≥ 2 overnight stays after surgery
- Age ≥ 40 years to ≤ 85 AND history of coronary artery disease (CAD), peripheral artery disease (PAD), cerebrovascular disease/stroke, insulin-dependent diabetes mellitus (IDDM), or chronic heart failure (CHF)
- Elective surgery
- Patients undergoing orthopaedic, traumatology, vascular, spinal, thoracic, neurosurgical, urological or visceral surgery
- Patient consent available
You may not qualify if…
- Patient's refusal
- Heart surgery, cardiac arrest, acute mycardial infarction (AMI), cardiac valve intervention, or cardiac catheter ablation within 14 days prior to surgery OR involvement of heart surgery at index surgery OR surgery planned on cardiopulmonary bypass
- Patients undergoing plastic/reconstructive, ophthalmologic, dental, hand surgery, or ear-nose-and-throat surgery
- Chronic renal failure on dialysis, unless undergoing renal transplant surgery
- Moderate to severe dementia
- Inclusion into study within the last year
Where it is running
- University Hospital Basel — Basel, Canton of Basel-City, Switzerland (enrolling)
Full record on ClinicalTrials.gov
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