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Clinical Trial Summary

Background and Objective: To evaluate the efficacy of cooled versus room temperature artificial tears in reducing post intravitreal injection (IVI) ocular discomfort. Patients and Methods: Patients receiving IVI were randomized to either cooled or room temperature tears intervention groups. Both groups rated their ocular discomfort following IVI before intervention and again after administration of cooled or room temperature tears.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05832996
Study type Interventional
Source University of Iowa
Contact
Status Completed
Phase Phase 4
Start date March 1, 2022
Completion date July 6, 2022

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