About this trial
This study is testing whether a special formula called Fortini, which is a high-calorie, low osmolality formula can help high-risk babies with single ventricle physiology grow better after their initial Stage 1 surgical palliation. These babies often struggle to gain weight, which can lead to more health problems before their next surgery.
After their first heart surgery, but prior to discharge, babies will be randomly placed into two groups. One group will get Fortini formula when they leave the hospital, and the other group will get the standard of care high-calorie formula. The primary goal is to see if Fortini helps babies grow better by the time they are ready for their second surgery.
The study will also check if the babies tolerate the formula well, how much they eat, how often they are re-admitted to the hospital, and how their caregivers feel about feeding. The babies will be followed for up to 4 months, until they return for their next surgery. About 100 infants are expected to join the study at Driscoll Children's Hospital.
This research may help improve nutrition care for infants with complex heart conditions and reduce stress for their families.
Eligibility criteria
Qualifiers
Infants with single ventricle physiology who have undergone Stage 1 surgical palliation (e.g., Norwood, hybrid, or BT shunt)
Medically stable and ready for discharge from the hospital
Feeding via oral, nasogastric (NG), or gastrostomy tube
Age < or = 6 months at time of discharge
Disqualifiers
Preexisting gastrointestinal condition contraindicating formula use (e.g. NEC, short gut, malabsorption)
Contraindication to Fortini (e.g. proven cow's milk protein allergy)
Current enrollment in another interventional feeding or nutrition study
Social circumstances likely to preclude safe outpatient follow up
Trial design
Treatments tested in this trial
- Fortini formula
- Standard Nutritional Care