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Consequences of Parenteral Nutrition Photoprotection on Oxidant Related Diseases Among Extremely Low Birth Weight Infants

Civil Hospices of Lyon logo

Civil Hospices of Lyon

Status

Completed

Conditions

Infant, Premature

Treatments

Device: standard tubing and bags
Device: photoprotected bags, tubing, syringes

Study type

Interventional

Funder types

Other

Identifiers

NCT00328419
2004.358

Details and patient eligibility

About

The antioxidant system of very low birth weight infants is immature. This immaturity is implicated in the pathogenesis of diseases such as bronchopulmonary dysplasia or retinopathy. The main source of oxidant is oxygen, and parenteral nutrition is contaminated with oxidant. Photoprotection decreases the oxidant load infused with parenteral nutrition. In a preliminary study, photoprotection reduced the frequency of pulmonary bronchodysplasia, increased the quantity of enteral nutrition tolerated, and decreased the arterial blood pressure among very low birth weight infants. The aim of this study is to evaluate the impact of photoprotection on oxidant related diseases among very low birth weight infants. This study is a randomized multicenter trial. In the intervention group, photoprotection is applied until the infusion of parenteral nutrition with amber bags, tubing, and syringes. The quality of photoprotection is controlled by measuring malondialdehyde and cysteine after 24 hours of infusion. The control group will receive parenteral nutrition with transparent bags and tubing. The outcomes are evaluated at 36 weeks, and 680 infants will be enrolled, with stratification among centers and gestational age.

Enrollment

591 patients

Sex

All

Ages

1 to 6 days old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Infants born before 30 weeks gestational age
  • Postnatal age between 1 and 6 days
  • Apgar score up to 2

Exclusion criteria

  • Severe congenital abnormalities
  • Intraventricular hemorrhage grade up to 2
  • Proven sepsis before inclusion
  • Transfusion before inclusion
  • Use of intravenous lipids or parenteral nutrition before randomisation

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

591 participants in 2 patient groups

1
Experimental group
Description:
photoprotected parenteral nutrition
Treatment:
Device: photoprotected bags, tubing, syringes
2
Active Comparator group
Description:
Non-photoprotected parenteral nutrition
Treatment:
Device: standard tubing and bags

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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