Clinical Trials Directory

Trials / Unknown

UnknownNCT00799721

Urine VEGF Levels in Very Low Birth Weight (VLBW) Infants

Status
Unknown
Phase
Study type
Observational
Enrollment
160 (estimated)
Sponsor
Charite University, Berlin, Germany · Academic / Other
Sex
All
Age
32 Weeks
Healthy volunteers
Not accepted

Summary

VLBW infants are at risk of developing retinopathy of prematurity (ROP). In the first phase of ROP there is a down-regulation of retinal VEGF-expression because of postnatal relative hyperoxia, followed by an upregulation of VEGF mediated through retinal hypoxia, which leads to pathologic vessel formation. VEGF acts through binding to the specific receptor FLT-1, the soluble form sFLT-1 is a specific antagonist of VEGF action. Erythropoietin, given to VLBW infants to prevent anemia, may stimulate VEGF-production in neuronal cells. Currently, there are no data published about VEGF urine-levels in VLBW infants and it is not known, if urine VEGF-levels may serve as a non-invasive marker of ROP-risk. Further shall be investigated, if erythropoietin-therapy increases urine VEGF-levels and if there is a correlation with ROP-development.

Conditions

Timeline

Start date
2008-08-01
Primary completion
2010-02-01
Completion
2010-12-01
First posted
2008-12-01
Last updated
2008-12-01

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00799721. Inclusion in this directory is not an endorsement.