Post-operative Cardiac Outcome of Non-cardiac Surgery Predicted by INVOS
NCT ID: NCT02079454
Last Updated: 2014-03-05
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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COMPLETED
34 participants
OBSERVATIONAL
2011-03-31
2013-12-31
Brief Summary
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The investigators postulate that a drop in the Invos numbers (with or without significant drop in BP) is associated with a variable degree of cardiac suffering.
The idea is to prevent per and foremostpost-operative myocardial necrosis complications by acting as soon as we have an INVOS drop during anesthesia.
The "cardiac events" will be monitored and defined according to the EHA (european heart association) guidelines.
(Changes of the EKG and/or troponin I values above the threshold). Patient will be monitored per and post operatively.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Age minimum 18 years old
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Cliniques universitaires Saint-Luc- Université Catholique de Louvain
OTHER
Responsible Party
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Locations
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cliniques universitaires St Luc
Brussels, Brabant, Belgium
Countries
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Other Identifiers
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invos0001
Identifier Type: -
Identifier Source: org_study_id
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