Trials / Completed
CompletedNCT00967486
Selective Versus Routine Shunting in Carotid Endarterectomy Patients
Selective Shunting in Appropriately Selected Patients Undergoing Carotid Endarterectomy Based on Stump Pressure
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 200 (actual)
- Sponsor
- CAMC Health System · Academic / Other
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Accepted
Summary
The project involves prospectively randomizing patients to either routine carotid shunting or selective carotid shunting during Carotid endarterectomy (CEA) under general anesthesia (GA) to see the difference in post-op complications and occurence rates. Patients will be randomized to Routine shunt vs selective groups.
Detailed description
The significance extends to all surgeons who perform Carotid endarterectomy because of their desire to improve patient care by decreasing the overall perioperative complication rate of the procedure by selectively not shunting those patients who ideally do not require it and thus eliminating the attendant morbidity associated with it. The hypothesis is that there will be no difference in patient outcomes (death, minor strokes, major strokes, transient ischemic attack (TIA)) for patients undergoing a Carotid endarterectomy with a SP of \> 50 mm Hg using selective shunting.Patients will be randomized to Routine shunt vs selective groups. In Selective shunt, there will be subgroup analysis to measure % stenosis if the systolic pressure is \< 40mmHg calling it as Shunt group. All patients in the study, irrespective of treatment group will be followed post-operatively from 24 hours to 30 days. The patient will be monitored and the following outcomes documented - death, minor stroke, major stroke, trans-ischemic attack (TIA).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Carotid endarterectomy with routine shount | |
| PROCEDURE | Carotid endarterectomy with selective shunt |
Timeline
- Start date
- 2006-12-01
- Primary completion
- 2009-06-01
- Completion
- 2009-06-01
- First posted
- 2009-08-28
- Last updated
- 2013-10-24
- Results posted
- 2013-10-24
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00967486. Inclusion in this directory is not an endorsement.