Monitoring of Vital Signs for Phenotyping of Perioperative Myocardial Infarction/Injury After Noncardiac Surgery
Recruiting
Observational Study
Perioperative Myocardial Infarction
Perioperative Myocardial Injury
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 40 – 85
- Sex
- Any
- Study type
- Observational
- Participants needed
- 875 (estimated)
- Sponsor
- University Hospital, Basel, Switzerland · Other
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About This Trial
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…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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 diabe…
Contacts