Fasudil Eye Drop in Retinopathy Of Prematurity(ROP)

Status Recruiting

Clinical Trial Summary

Eligible eyes are randomly assigned into two groups. Group A receive Fasudil eye drops (concentration 0.5 percent) twice daily. Group B, receive artificial tears drop with the same frequency. Retinal specialists who are expert in Retinopathy Of Prematurity field will perform fundus examination regularly. The examiners are blind. The progression of normal retinal vascularization and need to treatment will be documented and compared between the two study groups. The topical eye drops are used until the retinal vascularization are complete (45 week after LMP) or the patient needs to be treated.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04191954
Study type	Interventional
Source	Shahid Beheshti University of Medical Sciences
Contact	Alireza Ramezani, MD
Phone	009822591616
Email	labbafi@hotmail.com
Status	Recruiting
Phase	Phase 2/Phase 3
Start date	June 2, 2019
Completion date	September 2020

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See also
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