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Unraveling Perioperative Myocardial Injury

unRaveling pErioperative MyocArdial INjury

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06728111
Acronym
REMAIN
Enrollment
1114
Registered
2024-12-11
Start date
2023-07-24
Completion date
2027-03-01
Last updated
2024-12-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myocardial Injury, Myocardial Injury After Non-Cardiac Surgery

Brief summary

The aim of this study is to gain insight into the etiology of myocardial injury after non cardiac surgery. Furthermore, suspected etiologies were explored and hierarchically classified into most likely cause how this determines prognosis and what factors are associated with improved outcome.

Detailed description

As above

Interventions

OTHERHigh 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.

Sponsors

Erasmus Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 18 year of age * 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

* Re-operations within the study period. * Daycare surgery

Design outcomes

Primary

MeasureTime frameDescription
Main etiologies elevated troponin Tfrom enrollmentThe primary endpoint is a description of the main etiologies found within patients with an elevated troponin T after non cardiac surgery.

Secondary

MeasureTime frameDescription
Differences in adjudicationfrom enrollmentDifferences in the adjudication process between different doctors will be assessed according to intraclass coeficients and Fleisch Kappa

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026