Feeding After Neonate Surgery Review

This study has been terminated.
(sufficient data gathered for study conclusion)
Sponsor:
Information provided by:
Children's Healthcare of Atlanta
ClinicalTrials.gov Identifier:
NCT00229866
First received: September 13, 2005
Last updated: July 5, 2011
Last verified: July 2011
  Purpose

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
Congenital Disorders

Study Type: Observational
Study Design: Time Perspective: Retrospective
Official Title: Feeding After Neonatal Surgery Chart Review

Further study details as provided by Children's Healthcare of Atlanta:

Enrollment: 90
Study Start Date: August 2005
Study Completion Date: June 2006
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.

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Neonates who undergo cardiac surgery

Criteria

Inclusion Criteria:

  • Neonates who undergo cardiac surgery

Exclusion Criteria:

-

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00229866

Locations
United States, Georgia
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
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00229866     History of Changes
Other Study ID Numbers: 04-072
Study First Received: September 13, 2005
Last Updated: July 5, 2011
Health Authority: United States: Food and Drug Administration

Keywords provided by Children's Healthcare of Atlanta:
newborn
pediatric health
Feeding difficulty
discharge with a NG tube
G-tube placement
Nissen fundoplication

ClinicalTrials.gov processed this record on October 20, 2014