Registry for Severe ROP and Treatment on Visual Outcomes
NCT01559571 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 324
Last updated 2020-06-30
Summary
The purpose of this study is to determine what factors influence the visual outcomes of infants with severe retinopathy of prematurity (ROP) and to monitor the outcomes.
Conditions
- Retinopathy of Prematurity
Sponsors & Collaborators
-
Pediatrix
lead OTHER
Principal Investigators
-
Reese H Clark, MD · Pediatrix
Eligibility
- Max Age
- 7 Days
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2012-05-31
- Primary Completion
- 2020-05-15
- Completion
- 2020-05-15
Countries
- United States
Study Locations
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