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Nutritional Intervention for Preterm Infants-2

Nutritional Intervention for Preterm Infants-2

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON20272
Enrollment
240
Registered
2008-09-15
Start date
2008-10-06
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Preterm neonates, Premature infants, parenteral nutrition, tolerance

Interventions

Intervention group A will receive lipids from birth onwards. Interventiongroup B will receive extra amino acids in combination with lipids from birth onwards. The control group will be fed according t

Sponsors

Erasmus Medical Center - Sophia Children's Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Inborn, Gestational weight less than 1500g

Exclusion criteria

Exclusion criteria: 1. Congenital anomalies 2. Metabolic disease 3. Endocrine, renal or hepatic disorder

Design outcomes

Primary

MeasureTime frame
Nitrogen balance

Secondary

MeasureTime frame
1. Safety of the nutritional regimen: as reflected by normal blood chemistry, no effect on hearing ability, no effect on chronic lung disease; 2. Growth: measured in terms of body weight, knemometry, head circumference, protein accretion and protein breakdown; 3. Fatty acid profile in plasma and erythrocytes; 4. Energy expenditure; 5. Short- and long-term outcome: days on mechanical ventilation, incidence of bronchopulmonary dysplasia, incidence of infection, intraventricular hemorrhage, and necrotizing enterocolitis, normal ALGO-test and Bayley III scores

Contacts

Public ContactJ.B. Goudoever, van

Erasmus Medical Center, Sophia Children's Hospital P.O. Box 2060

j.vangoudoever@erasmusmc.nl+31 (0)10 4636363

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)