Clinical Trials Directory

Trials / Completed

CompletedNCT02230358

Cardiac Output and Duplex Sonography in Carotid Endarterectomy

Cardiac Output and Cerebral Blood-flow During Carotid Endarterectomy in Regional vs. General Anesthesia. A Prospective Randomized Controlled Single Center Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
90 (actual)
Sponsor
Medical University Innsbruck · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to investigate the differences between the cardiac output and the cerebral blood-flow between a regional anesthesia (RA) and a general anesthesia (GA) in a randomized, controlled, single center study at the Medical University Innsbruck, Department of Anesthesia and Intensive Care Medicine.

Detailed description

The investigators will investigate the differences between the cardiac output and the cerebral blood-flow between a regional anesthesia (RA) and a general anesthesia (GA) in a randomized, controlled, single center study at the Medical University Innsbruck, Department of Anesthesia and Intensive Care Medicine. For this purpose patients with the need of a carotid endarterectomy (CEA) will be included and randomized either to the regional anesthesia (RA) or the general anesthesia (GA) group until a patient number of 45 in each group is achieved. The cardiac output and cerebral blood-flow via trans-cranial Doppler (TCD) will be measured at 6 time points: * T0 Baseline (after insertion of an arterial line) * T1 After induction of anesthesia, but before surgical start * T2 Two minutes after clamping the carotid artery * T3 Two minutes after shunt insertation of the carotid artery * T4 After reperfusion * T5 After completion of the skin suture

Conditions

Interventions

TypeNameDescription
PROCEDURERegional anesthesiaRegional anesthesia
PROCEDUREGeneral anesthesiaGeneral anesthesia
DEVICETranscranial Doppler ultrasonography6x for 4 hours
PROCEDUREblood gas analysis6 x 3 ml blood withdrawal (18 ml) within 4 hours
PROCEDUREinvasive arterial blood pressure measurementbefore operation, 8 hours, as done in clinical routine
PROCEDUREarterial blood gas measurementperioperative, 4-6 times within 8 hours, as done in clinical routine
BEHAVIORALNeurological Controlperioperative, 2-3 days, as done in clinical routine
BEHAVIORALNIRS monitoringperioperative, for 5 hours, as done in clinical routine
DEVICEoxygen supply (not invasive 'Vigileo')perioperative for 5 hours, as done in clinical routine

Timeline

Start date
2014-07-01
Primary completion
2017-07-01
Completion
2017-07-01
First posted
2014-09-03
Last updated
2021-09-13

Locations

1 site across 1 country: Austria

Source: ClinicalTrials.gov record NCT02230358. Inclusion in this directory is not an endorsement.