Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
1114 participants
OBSERVATIONAL
2023-07-24
2027-03-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Interventions
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High sensitive Troponin T
The baseline population will consist of all patients who underwent a form of non-cardiac surgery. Baseline variables, medication use, type of surgery and perioperative hemodynamic and laboratory variables will be extracted from the hospital information system. One year mortality is registered, as well as major vascular events. This is in line with previous publications from our group. The adjudication strategy used for patients with myocardial injury. For the adjudication process minimal two senior anesthesiologists will be invited. Two members with at least one senior anesthesiologist will receive a sample of patients to adjudicate. Together the entire panel will adjudicate all patients. The goal to investigate the differences between the raters.
Eligibility Criteria
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Inclusion Criteria
* Undergoing non-cardiac surgery in the Erasmus MC, with (high-sensitive) Troponin T \> 50 ng/L measured in any of the first three days after surgery.
Exclusion Criteria
* Daycare surgery
18 Years
ALL
No
Sponsors
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Erasmus Medical Center
OTHER
Responsible Party
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Felix van Lier
Anesthesiologist
Principal Investigators
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Sanne Hoeks, PhD
Role: STUDY_DIRECTOR
Epidemiologist
Felix van Lier, PhD
Role: PRINCIPAL_INVESTIGATOR
Anesthesiologist
Locations
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Erasmus Medical Center
Rotterdam, , Netherlands
Countries
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Provided Documents
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Document Type: Study Protocol
Other Identifiers
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10945
Identifier Type: -
Identifier Source: org_study_id