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Monitoring of Vital Signs for Phenotyping of Perioperative Myocardial Infarction/Injury After Noncardiac Surgery

NCT05866874 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 875

Last updated 2025-01-28

No results posted yet for this study

Summary

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.

Conditions

  • Perioperative Myocardial Infarction
  • Perioperative Myocardial Injury

Sponsors & Collaborators

  • University Hospital, Basel, Switzerland

    lead OTHER

Principal Investigators

  • Christian Müller, MD, Prof · University Hospital, Basel, Switzerland

Eligibility

Min Age
40 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-20
Primary Completion
2025-12-31
Completion
2026-12-31

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05866874 on ClinicalTrials.gov