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Risk Factors of Breastfeeding Study
This study has been completed.
Sponsored by: Children's Mercy Hospital Kansas City
Information provided by: Children's Mercy Hospital Kansas City
ClinicalTrials.gov Identifier: NCT00195962
  Purpose

The goal of this study is to identify infants who are at risk for developing problems related to being breast-fed.


Condition
Healthy

MedlinePlus related topics: Breast Feeding
U.S. FDA Resources
Study Type: Observational
Study Design: Case-Only, Prospective
Official Title: Identification of Risk Factors Among Breast-Fed Infants

Further study details as provided by Children's Mercy Hospital Kansas City:

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 1500
Study Start Date: June 2004
Study Completion Date: June 2007
Primary Completion Date: June 2007 (Final data collection date for primary outcome measure)
Detailed Description:

The goal of this study is to identify infants who are at risk for developing problems related to being breast-fed. A previous study identified items that place an infant at a high risk for developing complications related to being breast-fed. The present study will use the same survey and collect data from more participants. These additional participants are necessary to provide statistical analysis for the survey. The survey being developed will assist health care professionals to identify those infants at risk for developing health problems related to being breast-fed and provide care that will minimize the chances of developing complications.

  Eligibility

Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
  • Mothers of healthy infants that are breastfeeding
  • At least 24 hours post delivery
  • Mother and baby will be dismissed from the hospital together.
Criteria

Inclusion Criteria:

  • Mothers of healthy infants that are breastfeeding
  • At least 24 hours post delivery
  • Mother and baby will be dismissed from the hospital together.

Exclusion Criteria:

  • Mothers of newborns that are not breastfeeding
  • Mothers of newborns that are ill and/or will not be dismissed from the hospital at the same time as the mother
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00195962

Locations
United States, Missouri
Truman Medical Center - Hospital Hill
Kansas City, Missouri, United States, 64108
Truman Medical Center - Lakewood
Lee's Summit, Missouri, United States, 64139
Children's Mercy Hospitals and Clinics
Kansas City, Missouri, United States, 64108
Sponsors and Collaborators
Children's Mercy Hospital Kansas City
Investigators
Principal Investigator: Anne Mercer, RN Children's Mercy Hospital Kansas City
  More Information

Publications:
Responsible Party: Children's Mercy Hospitals and Clinics ( Susan Teasley, RN, CCRC )
Study ID Numbers: 040107
Study First Received: September 13, 2005
Last Updated: December 17, 2008
ClinicalTrials.gov Identifier: NCT00195962  
Health Authority: United States: Institutional Review Board

Keywords provided by Children's Mercy Hospital Kansas City:
Breastfeeding
Post-partum mothers of healthy breast-fed newborns

Study placed in the following topic categories:
Healthy

ClinicalTrials.gov processed this record on January 16, 2009