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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Regional anesthesia | Regional anesthesia |
| PROCEDURE | General anesthesia | General anesthesia |
| DEVICE | Transcranial Doppler ultrasonography | 6x for 4 hours |
| PROCEDURE | blood gas analysis | 6 x 3 ml blood withdrawal (18 ml) within 4 hours |
| PROCEDURE | invasive arterial blood pressure measurement | before operation, 8 hours, as done in clinical routine |
| PROCEDURE | arterial blood gas measurement | perioperative, 4-6 times within 8 hours, as done in clinical routine |
| BEHAVIORAL | Neurological Control | perioperative, 2-3 days, as done in clinical routine |
| BEHAVIORAL | NIRS monitoring | perioperative, for 5 hours, as done in clinical routine |
| DEVICE | oxygen 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.