Preterm Infants Clinical Trial
Official title:
Study of the Oxidant-Antioxidant Effects of Parenteral Nutrition in Preterm Neonates
Verified date | January 2008 |
Source | Mansoura University |
Contact | n/a |
Is FDA regulated | No |
Health authority | Egypt: Ministry of Health and Population |
Study type | Interventional |
In an effort to decrease the load of peroxides in TPN solutions, multiple studies examined different strategies such as photo-protection, adding multivitamins to the lipid emulsion rather than to the dextrose-amino acid admixture, and adding antioxidants such as glutathione to the TPN solution. However, the role of trace elements as antioxidants, and their interaction with light have not been studied. Also, the impact of TPN-related oxidants on clinical morbidities has not been addressed. Therefore, we aimed in this study of preterm infants to evaluate the role of different components of TPN on urinary peroxides and to examine the biochemical and clinical effects of light protection.
Status | Completed |
Enrollment | 80 |
Est. completion date | January 2005 |
Est. primary completion date | January 2005 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A to 7 Days |
Eligibility |
Inclusion Criteria: Preterm infants included are: 1. with gestational age between 28 to 34 weeks 2. managed with TPN as part of their care in the NICU 3. their postnatal age on enrolment was < 7 days Exclusion Criteria: Infants are excluded if they have: 1. Clinical evidence of sepsis, or a positive blood culture on admission 2. Hepatobiliary dysfunction 3. Persistent metabolic acidosis with base deficit > 10 mEq / L 4. Renal impairment (urine output < 1 ml/kg/hour and serum creatinine > 1 mg/dl) 5. Disseminated intravascular coagulopathy 6. Maternal conditions known to be associated with oxidative stress such as preeclampsia, hypertension and diabetes. |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Mansoura University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Concentration of peroxides in the urine | 48 hours | No | |
Secondary | Clinical morbidities (death, and bronchopulmonary dysplasia) | during hospital stay | Yes |
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