Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DEVICE | NIRS - 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.