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A Safety and Efficacy Assessment of Resolvine for Treatment of Vitreomacular Attachment

Vitreomacular Traction Clinical Trial

Official title:
A Safety and Efficacy Assessment of Resolvine for Treatment of Vitreomacular Attachment

Clinical Trial Summary

This research is studying the effect that Resolvine injection will have on patients with vitreomacular adhesion.

Clinical Trial Description

This research is studying the effect that Resolvine injection will have on patients with vitreomacular adhesion. The investigators propose that intravitreal injection of Resolvine® 36% will: 1)Result in release of the vitreous adhesion to the macula in subjects with symptomatic vitreomacular attachment (VMA). 2)The Release of the VMA will create a measurable and favorable retinal change. 3) The release of vitreomacular traction may also result in visual acuity improvement within the short time frame of this study. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01966328
Study type Interventional
Source Ophthalmic Consultants of Boston
Contact
Status Active, not recruiting
Phase Phase 1
Start date October 2013
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