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Trials / Terminated

TerminatedNCT00607061

Synthesis of Glutathione From Low Birth Weight Newborn Babies

Synthesis of Glutathione in Erythrocytes From Low Birth Weight Newborn Babies : Effect of Cysteine in Vitro

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
35 (actual)
Sponsor
Nantes University Hospital · Academic / Other
Sex
All
Age
9 Months
Healthy volunteers
Not accepted

Summary

The aim of the study is to determine mechanisms leading to glutathione deficiency in low birth weight newborn babies. Compared to full term neonates, depletion in this population may be due to a decreased synthesis rate or to an enhanced utilization or a combination of both mechanisms.The protocol is constituted of two steps. The objective of the first step is to quantify the blood concentration of glutathione in the artery and the vein of umbilical cord in full term newborn babies. Objectives of the second step are to determine if the glutathione synthesis rate, measured in vitro, is lower in erythrocytes collected from umbilical cord blood of low weight newborn babies compared to full term newborn babies. In this case, the next objective will be to determine if the adjunction of an excess of cysteine in vitro can restore the glutathione synthesis rate in these cells.

Conditions

Interventions

TypeNameDescription
PROCEDUREBlood sample collectionBlood of the umbilical cord will be collected after delivery. A mother blood sample will be also collected in the few hours preceding delivery to determine glutathione and cysteine concentrations.

Timeline

Start date
2007-10-01
Primary completion
2010-07-01
Completion
2010-07-01
First posted
2008-02-05
Last updated
2013-09-30

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT00607061. Inclusion in this directory is not an endorsement.

Synthesis of Glutathione From Low Birth Weight Newborn Babies (NCT00607061) · Clinical Trials Directory