RecruitingNot ApplicableNCT06915922

YAG Laser Vitreolysis for Vitreous Floaters

Therapeutic Neodymium-doped Yttrium-Aluminum-Garnet (Nd:YAG) Laser Vitreolysis for Vitreous Floaters - A Study to Quantify Visual Quality of Life, Vitreous Structure, and Vision Before and After Nd:YAG Laser Vitreolysis in Patients With Vision Degrading Myodesopsia


Sponsor

VMR Consulting, Inc.

Enrollment

50 participants

Start Date

Oct 17, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to measure how the quality of life, the structure of eye, and vision change after treatment for the opacities in the gel (vitreous) that fills the center of eye which cause vision disturbances commonly called "floaters". In this study the vitreous floaters are treated using a Neodymium-doped yttrium-aluminum-garnet (Nd:YAG) laser. The FDA has approved the use of this laser to treat membranes in the eye.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Neodymium-doped yttrium-aluminum-garnet (Nd:YAG) laser therapy for people with myopic vitreopathy, posterior vitreous detachment, and other related conditions. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICENeodymium-doped yttrium-aluminum-garnet (Nd:YAG) laser therapy

Nd:YAG laser treatment(s) for Vision Degrading Myodesopsia (clinically significant vitreous floaters) in eyes with vitreous opacities due to myopic vitreopathy and posterior vitreous detachment (PVD).


Locations(1)

VMR Institute for Vitreous Macula Retina

Huntington Beach, California, United States

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NCT06915922


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