Refractive Error and Biometry in Retinopathy of Prematurity

NCT03334513 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 35

Last updated 2017-11-07

No results posted yet for this study

Summary

The investigators compared long-term refractive and biometric outcomes in children with retinopathy of prematurity who received two different anti-vascular endothelial growth factor agents.

Conditions

  • Retinopathy of Prematurity

Interventions

DRUG

Bevacizumab

intravitreal injection of bevacizumab

DRUG

Ranibizumab

intravitreal injection of ranibizumab

Sponsors & Collaborators

  • San Ni Chen

    lead OTHER

Eligibility

Min Age
3 Years
Max Age
3 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-04-01
Primary Completion
2014-04-01
Completion
2014-04-01
FDA Drug
Yes

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03334513 on ClinicalTrials.gov