Nutritional Study in Preterm Infants

Completed · Phase 3

Conditions studied: Preterm Infants

In brief

An evaluation of a preterm infant formula containing ingredients similar to those found in breastmilk

Key facts

Study ID

NCT00707837

Run by

Abbott Nutrition

People needed

206

Starts

2005-05-01

Expected to finish

2008-08-01

Last updated by the study team

2009-04-27

Who can join

Age: any, up to 0. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Birthweight 500-1800 g
• Less than 33 wks gestational age
• Enteral feeding initiated by 21 days of life
• Asymmetrical small-for-gestational age (SGA) infants and infants with patent ductus arteriosus (PDA) are eligible to participate
• Singleton or twin births only
• Infant is 21 days of age or less at time of randomization

You may not qualify if…

• Serious congenital abnormalities that may affect growth and development
• Grade III or IV intraventricular hemorrhage (IVH)
• Maternal incapacity
• History of major surgery
• Extracorporeal membrane oxygenation (ECMO)
• Asphyxia
• Confirmed NEC or positive blood cultures at the time of randomization

Where it is running

• University of Alabama — Birmingham, Alabama, United States
• West Coast Neonatalogy, All Children's Hospital — St. Petersburg, Florida, United States
• University of South Florida — Tampa, Florida, United States
• University of Louisville — Louisville, Kentucky, United States
• Maria Fareri Children's Hospital at Winchester Medical Center — Vahalla, New York, United States
• MetroHealth Medical Center — Cleveland, Ohio, United States
• Women & Infants Hospital of Rhode Island — Providence, Rhode Island, United States
• University of Utah — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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