Post-operative Cardiac Outcome of Non-cardiac Surgery Predicted by INVOS

Valeur Predictive de l'INVOS Sur l'Outcome Cardiaque en Post-opératoire. (French Title)

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02079454

Enrollment

Registered

2014-03-05

Start date

2011-03-31

Completion date

2013-12-31

Last updated

2014-03-05

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

Conditions

Cardiac Outcome, Invos, Peri-operative

Brief summary

Research aimed to find a correlation with an invos drop and cardiac events in the peri-operative period of non cardiac surgery. 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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Male and female * Age minimum 18 years old

Exclusion criteria

* Chronic renal failure

Design outcomes

Primary

Measure	Time frame	Description
A composite measurement of major vascular events in the post-operative period	96 hours post-operative	Myocardial infarction (measured by positivation of troponin I assay above the defined threshold) associated with clinical data (pain, dyspnea,...) or ST modification on the EKG or apparition of a new LBBB, or new wall abnormalities on the TTE. Or new TIAs or CVAs

Countries

Belgium

Outcome results