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Clinical Trial Summary

We hypothesize that topical betaxolol will reduce the development of severe retinopathy of prematurity.


Clinical Trial Description

The drug is administered twice a day between 32 and 35 weeks gestational age, at a t ime when ROP is most likely to arise. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT01660620
Study type Interventional
Source Smith-Kettlewell Eye Research Institute
Contact
Status Completed
Phase Phase 1
Start date April 2011
Completion date November 2011