CEA: Neuropsychometric Outcome After Carotid Endarterectomy

Sponsor
Columbia University (Other)
Overall Status
Completed
CT.gov ID
NCT00597883
Collaborator
(none)
585
1
139
4.2

Study Details

Study Description

Brief Summary

The purpose of this study is to determine how well patients undergoing carotid endarterectomy will perform on a battery of tests to assess brain function before and after surgery as compared to a control group of patients undergoing spine surgery. This study will serve to: (a) determine incidence of neurologic/neuropsychometric change in patients undergoing carotid artery surgery, and (b) to ascertain the time it takes for these changes to resolve.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Cerebral injury will be determined in four ways. First, all patients will be evaluated using a battery of neuropsychometric tests before and after surgery. Patients admitted to the Irving Clinical Research Center (CRC) will have their tests one day before, one day after surgery and at 1 month. Those coming into the hospital on the day of surgery, "Same Day", will be evaluated on the day of surgery, one day after and at the 1 month follow up. Preoperative neurological and neuropsychological evaluation will be performed. The neuropsychometric tests are not intended to be diagnostic of specific neuropsychiatric disorders, but rather are designed to demonstrate general neuropsychological pathology. These tests can be divided into four types: (1) an evaluation of language, (2) an evaluation of speed of mental processing, (3) an evaluation of ability to learn using a list of words, and (4) an evaluation of visual perception requiring a patient to copy a complex figure. Before the battery is administered we will assess each patient's level of pain while sitting and standing using a 10 point Visual Analog Scale and then gauge their mood with a series called the Wong/Baker Faces Rating scale.

    We will be measuring Quality of Life (QOL) in all enrolled patients. This will be done using two well-known examinations (Telephone Interview for Cognitive Status (TICS) and Centers for Disease Control and Prevention Health-Related Quality of Life 14 Item Measure (CDC HRQOL14)) and a series of questions investigating how well patients are able to perform activities of daily living (ADLs) and instrumental activities of daily living (IADLs). These tests will be given at two time points, once before the surgery and then one month after surgery. We will look for changes in quality of life that may correlate with neuropsychometric test performance.

    Peripheral serum samples will be drawn before induction, before cross-clamping the carotid artery, 15 minutes after cross-clamping the carotid artery and 24 hours after surgery. These samples will be analyzed for four different sets of markers of cerebral injury, one gene and two markers of systemic inflammation. Serum levels of neuron specific enolase (NSE) and protein S100B, a neuronal enzyme and glial cell component respectively, markers of cell injury will demonstrate cerebral injury

    Patients will undergo intraoperative TCD (Transcranial Doppler) The TCD examination will assess the brain's ability to increase cerebral blood flow in response to a pharmacological challenge (CO2 inhalation). TCD measures the degree of cerebral vasodilation, identified as an increase in flow velocity on TCD. This "cerebrovascular reserve" we hypothesize will be able to predict performance on postoperative neuropsychometric tests

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    585 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Neurologic and Neuropsychometric Outcome in Patients Undergoing Carotid Endarterectomy
    Study Start Date :
    Mar 1, 2003
    Actual Primary Completion Date :
    Oct 1, 2014
    Actual Study Completion Date :
    Oct 1, 2014

    Outcome Measures

    Primary Outcome Measures

    1. Neuropsychometric Changes [Baseline to 1 Day]

    Secondary Outcome Measures

    1. Neuropsychometric Changes [Baseline to 1 Month]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • ability to speak English

    • undergoing carotid endarterectomy procedure

    • undergoing lumbar laminectomy procedure

    Exclusion Criteria:
    • history of permanent neurological impairment

    • Axis I psychiatric diagnosis or drug abuse

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Columbia University, Department of Anesthesiology New York New York United States 10032

    Sponsors and Collaborators

    • Columbia University

    Investigators

    • Principal Investigator: Eric J Heyer, M.D., Ph.D., Columbia University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Eric J. Heyer, MD, PhD, Professor of Clinical Anesthesiology, Columbia University
    ClinicalTrials.gov Identifier:
    NCT00597883
    Other Study ID Numbers:
    • AAAA4811
    First Posted:
    Jan 18, 2008
    Last Update Posted:
    Feb 5, 2015
    Last Verified:
    Feb 1, 2015
    Keywords provided by Eric J. Heyer, MD, PhD, Professor of Clinical Anesthesiology, Columbia University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 5, 2015