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To Assess the Efficacy of Early Administration of Energy Enriched and Protein Enriched Formula in Post Cardiac Repair Infants: a Randomized Controlled Trial, Comparative Study

To Assess the Efficacy of Early Administration of Energy Enriched and Protein Enriched Formula in Post Cardiac Repair Infants: a Randomized Controlled Trial, Comparative Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05826769
Enrollment
60
Registered
2023-04-24
Start date
2021-07-21
Completion date
2024-03-12
Last updated
2023-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congenital Heart Disease in Children, Malnutrition, Infant, Post-cardiac Surgery

Keywords

Energy Protein, Enriched, Enteral Nutrition, Cardiac Repair

Brief summary

Congenital heart disease (CHD) is a public health problem, A substantial percentage of infants and toddlers with CHD undergo cardiopulmonary bypass surgery. Undernutrition affects up to 90% of these patients, and it's contributed to worse surgical and neurological outcomes. Infants with CHD are typically delivered at full term with a normal birth weight. However, as time passes, their development may become stunted. There are no negotiated guidelines for nutritional monitoring and intervention in this age bracket of infants. Through the use of Energy Enriched and Protein Enriched nutrition formula during the postoperative phase, this has shown to be well tolerated and support in delivering higher nutrition intakes within the first days after surgery. The objective of this research is to assess the long term outcome of patients who have had energy- and protein-rich nutrition formulas post cardiac surgery. An open, 2-arm, randomized controlled trials will be conducted to assess the efficacy of early administration of energy enriched and protein enriched formula in post cardiac repair infants. The expected primary outcome is that intervention group will have good tolerance to feeding and the secondary outcome is the significant weight gain rate (weight velocity) in comparing to control groups

Detailed description

Due to a high incidence of 9/1000 live births, congenital heart disease (CHD) is a public health problem, A substantial percentage of infants and toddlers with CHD undergo cardiopulmonary bypass surgery. Undernutrition affects up to 90% of these patients, and it's contributed to worse surgical and neurological outcomes. Infants with CHD are typically delivered at full term with a normal birth weight. However, as time passes, their development may become stunted. There are no negotiated guidelines for nutritional monitoring and intervention in this age bracket of infants. Through the use of Energy Enriched and Protein Enriched nutrition formula during the postoperative phase, this has shown to be well tolerated and support in delivering higher nutrition intakes within the first days after surgery. Numerous clinical trials have been conducted (Zhang H et al., 2018; Scheeffer. et al., 2019) and were designed to explore the effects of early introduction of Energy Enriched and Protein Enriched formula (EP) to infants with CHD. The research found that feeding EP is correlated with improved weight gain and nutritional status, and also a decrease in Hospital Length Of Stay (HLOS) as well as antibiotic use, but this also causes increased feeding discomfort. The signs of feeding discomfort, on the other hand, were improved by medication and had little effect on feeding progress. The objective of this research is to assess the long term outcome of patients who have had energy- and protein-rich nutrition formulas post cardiac surgery.

Interventions

DIETARY_SUPPLEMENTEnergy- Protein Enriched Nutritional Formula

EN volume will start at 1 mL/kg/h and then increase by 1 mL/kg every 6 hours if tolerated, until reaching 130 mL/kg/d.

Sponsors

King Faisal Specialist Hospital & Research Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

According to national regulations, distribution of infant formula inside the hospital without a proper label is not allowed; therefore, subjects can not be blinded in this study.

Intervention model description

* Patients are randomized before surgery in blocks of 2 using a computer-generated randomization list into intervention and control groups * This will be An open, 2-arm,randomized controlled trial

Eligibility

Sex/Gender
ALL
Age
4 Weeks to 1 Years
Healthy volunteers
No

Inclusion criteria

1. infants born at term, age between 4 weeks and 12 months 2. post congenital heart surgery (RACHS score 2)

Exclusion criteria

1. syndromic patients 2. if patient is on parenteral nutrition (PN) 3. premature 4. combined inherited metabolic or chromosomal diseases 5. liver and kidney dysfunction before enrollment (index \>2 times the upper limit of normal) 6. upper GI activity, vomiting, diarrhea, bloating, and other symptoms before enrollment 7. breastfeeding patients. 8. cow's milk allergy

Design outcomes

Primary

MeasureTime frameDescription
after admission in ICU, will measure the Tolerability5 daysGastric tolerance

Secondary

MeasureTime frameDescription
Weight gain rate90 daysWeight velocity

Countries

Saudi Arabia

Contacts

Primary ContactAbrar Shirbini
ashirbini@kfshrc.edu.sa00966126677777
Backup ContactAhmed Elmahrouk
ael-mahrouk@kfshrc.edu.sa00966126677777

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026