Feeding Study in Premature Infants
- Conditions
- Premature Infants
- Interventions
- Other: Liquid human milk fortifierOther: Powder human milk fortifier
- Registration Number
- NCT00681018
- Lead Sponsor
- Mead Johnson Nutrition
- Brief Summary
To evaluate weight gain of preterm infants fed fortified human milk.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 143
- premature infant
- birth weight less than/equal to 1250 g
- exclusively breast fed
- metabolic or chronic disease
- major surgery
- ventilator dependent
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description 1 Liquid human milk fortifier Liquid human milk fortifier 2 Powder human milk fortifier Powder human milk fortifier
- Primary Outcome Measures
Name Time Method Weight gain 28 days
- Secondary Outcome Measures
Name Time Method Feeding tolerance 28 days
Trial Locations
- Locations (13)
Forsyth Medical Center
🇺🇸Winston-Salem, North Carolina, United States
The University of Arkansas for Medical Sciences
🇺🇸Little Rock, Arkansas, United States
Plantation General Hospital
🇺🇸Plantation, Florida, United States
University of Florida
🇺🇸Jacksonville, Florida, United States
Queen's Hospital
🇺🇸Jamaica, New York, United States
Advocate Hope Children's Hospital
🇺🇸Oak Lawn, Illinois, United States
All Children's Hospital
🇺🇸St. Petersburg, Florida, United States
Children's Hospital
🇺🇸Omaha, Nebraska, United States
Pitt County Memorial Hospital
🇺🇸Greenville, North Carolina, United States
SEAHEC
🇺🇸Wilmington, North Carolina, United States
Fairfax Hospital
🇺🇸Falls Church, Virginia, United States
Virginia Commonwealth University
🇺🇸Richmond, Virginia, United States
Advocate Lutheran General Children's Hospital
🇺🇸Park Ridge, Illinois, United States