Feeding After Neonate Surgery Review

Sponsor
Children's Healthcare of Atlanta (Other)
Overall Status
Terminated
CT.gov ID
NCT00229866
Collaborator
(none)
90
1
10
9

Study Details

Study Description

Brief Summary

The purpose is to determine what factors, if any, lead to delayed feeding, discharge with a NG tube, G-tube placement or Nissen fundoplication.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The purpose is to determine what factors, if any, lead to delayed feeding, discharge with a NG tube, G-tube placement or Nissen fundoplication. Will review the newborn database (Lumedx as most interested in those children who have never been fed prior to their cardiac surgery. The medical charts will be reviewed at Children's Healthcare of Atlanta at Egleston Hospital. Approximately 90 charts will be reviewed for newborns undergoing surgery in the 2003 calendar year.

    The factors that will be reviewed are pre-op feeding regimen, diagnosis, single vs two ventricle, open vs closed heart procedure, length of bypass, level of hypothermia, circulatory arrest, presence of TEE probe and post-op ventilation.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    90 participants
    Time Perspective:
    Retrospective
    Official Title:
    Feeding After Neonatal Surgery Chart Review
    Study Start Date :
    Aug 1, 2005
    Actual Study Completion Date :
    Jun 1, 2006

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      N/A and Older
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      No
      Inclusion Criteria:
      • Neonates who undergo cardiac surgery
      Exclusion Criteria:

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 Children's Healthcare of Atlanta Atlanta Georgia United States 30322

      Sponsors and Collaborators

      • Children's Healthcare of Atlanta

      Investigators

      • Principal Investigator: Brian Kogon, MD, Emory University

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00229866
      Other Study ID Numbers:
      • 04-072
      First Posted:
      Sep 30, 2005
      Last Update Posted:
      Jul 6, 2011
      Last Verified:
      Jul 1, 2011

      Study Results

      No Results Posted as of Jul 6, 2011