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Registry for Perioperative Data in Patients Undergoing Cardiac Surgery

Sponsor
Seoul National University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01713192
Collaborator
(none)
300
Enrollment
1
Location
20
Duration (Months)
15
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this registry is to obtain perioperative data in patients undergoing cardiac surgery and find out relations between the data and investigate several causes affecting postoperative complications.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    300 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Study Start Date :
    Jan 1, 2013
    Actual Primary Completion Date :
    Sep 1, 2014
    Actual Study Completion Date :
    Sep 1, 2014

    Arms and Interventions

    Arm Intervention/Treatment
    Cardiac surgery

    Outcome Measures

    Primary Outcome Measures

    1. perioperative data [1 year after surgery]

      To obtain the perioperative data in patients undergoing cardiac surgery. Data will be collected including demographics, surgery and postoperative complications. In addition, laboratory data such as coagulation and cytokine will be obtained. Intraoperative monitoring including bispectral index, cerebral oximeter, tissue oxygen saturation [InspectraTM StO2 (Hutchinson Technology Inc., MN, USA)], cardiac index [FloTrac/EV1000 (Edwards Lifesciences, Irvine, CA, USA), VolumeView/EV1000 (Edwards Lifesciences, Irvine, CA, USA), Vigilance II (Edwards Lifesciences, Irvine, CA, USA)] and mixed venous oxygen saturation will be evaluated.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • patients undergoing cardiac surgery
    Exclusion Criteria:
    • refused to participate

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Seoul National University Hospital Seoul Korea, Republic of

    Sponsors and Collaborators

    • Seoul National University Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Yunseok Jeon, Associate Professor, Seoul National University Hospital
    ClinicalTrials.gov Identifier:
    NCT01713192
    Other Study ID Numbers:
    • YSJeon_Registry
    First Posted:
    Oct 24, 2012
    Last Update Posted:
    Nov 18, 2015
    Last Verified:
    Nov 1, 2015

    Study Results

    No Results Posted as of Nov 18, 2015