Skip to content

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00799721
Enrollment
160
Registered
2008-12-01
Start date
2008-08-31
Completion date
2010-12-31
Last updated
2008-12-01

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

Conditions

Infant, Very Low Birth Weight

Keywords

ROP, VLBW, Epo, IUGR, VEGF, sFLT-1, very low birth weight infants, retinopathy of prematurity, erythropoietin therapy and risk of ROP

Brief 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.

Interventions

None listed

Sponsors

Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 32 Weeks
Healthy volunteers
No

Inclusion criteria

* gestational age \< 32 weeks * birth weight \<1500g

Exclusion criteria

* absent written consent by parents * connatal eye malformation

Design outcomes

Primary

MeasureTime frame
Development of ROP4 months

Countries

Germany

Contacts

Primary ContactAnke Reinhold, Doctor
anke.reinhold@charite.de+49/177/2950661
Backup ContactAnja Pohl-Schickinger, Doctor
anja.pohl@charite.de+49/30/450566122

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026