Cardiac Output Monitoring in Aortic Aneurysm Surgery

Sponsor
NHS Lothian (Other)
Overall Status
Completed
CT.gov ID
NCT01094938
Collaborator
(none)
30
1
12
2.5

Study Details

Study Description

Brief Summary

To compare CO values obtained by the lithium indicator dilution method and pulse power analysis before, during and after anaesthesia and surgery for the elective repair of abdominal aortic aneurysms. This will enable us to determine how often and when calibration of the pulse power analysis derived CO is required.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    30 participants
    Study Start Date :
    Jul 1, 2007
    Actual Primary Completion Date :
    Jul 1, 2007
    Actual Study Completion Date :
    Jul 1, 2008

    Arms and Interventions

    Arm Intervention/Treatment
    Repair

    Outcome Measures

    Primary Outcome Measures

    1. Cardiac output []

    Secondary Outcome Measures

    1. Arterial Pressure []

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients presenting for elective abdominal aortic and extent 4 thoracoabdominal aortic aneurysm repair
    Exclusion Criteria:
    • Patients not giving informed consent.

    • Patients under the age of 18 years.

    • Patients who may be pregnant

    • Patients with learning disabilities.

    • Rhythm other than sinus rhythm.

    • Patients on oral lithium therapy.

    • Patients less than 40kg

    • Patients with severe mitral regurgitation

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 NHS Lothian Edinburgh United Kingdom EH16 4SA

    Sponsors and Collaborators

    • NHS Lothian

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT01094938
    Other Study ID Numbers:
    • EDICOAAS
    • 07/S1102/30
    First Posted:
    Mar 29, 2010
    Last Update Posted:
    Mar 29, 2010
    Last Verified:
    Mar 1, 2010
    Keywords provided by , ,
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 29, 2010