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UnknownNCT02203370

Cerebral Oximetry for Carotid EEA

Status
Unknown
Phase
Study type
Observational
Enrollment
126 (estimated)
Sponsor
Salzburger Landeskliniken · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Aim oft he study is to compare two different devices for cerebral oximetry (FORE-SIGHTTM Monitor (CAS Medical Systems, Branford, Connecticut, USA and INVOSTM Somanetics, Troy, Michigan, USA) in patients undergoing surgical carotid thrombendarterectomy (cTEA) with crossclamped internal carotid artery (ACI). All procedures will be performed in regional anesthesia, therefore the patients will be awake and direct neurological examination during the procedure will be possible, giving information how the drop in cerebral saturation (measured with INVOS and FORESIGHT both on the same patient) correlates with any clinical symptoms. We expect to see a difference in the total drop and in the delay of the drop of cerebral oxygen saturation, making it possible to detect varieties in specificity and sensitivity of both devices compared to neurologic examination in the awake patient.

Conditions

Interventions

TypeNameDescription
DEVICENIRS - Near-infrared spectroscopy

Timeline

Start date
2014-07-01
Primary completion
2015-07-01
Completion
2016-12-01
First posted
2014-07-29
Last updated
2015-05-20

Locations

1 site across 1 country: Austria

Source: ClinicalTrials.gov record NCT02203370. Inclusion in this directory is not an endorsement.