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Study identifier: NCT06915922 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

YAG Laser Vitreolysis for Vitreous Floaters

Condition: Posterior Vitreous Detachment · Myopic Vitreopathy · VISION DEGRADING MYODESOPSIA  ·  Sponsor: VMR Consulting, Inc.

PhaseNA
Planned participants50
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Dr Jerry Sebag, MD, FACS, FRCOphth, FARVO  ·  714-901-7777  ·  JSebag@vmrinstitute.com

Always discuss trial participation with your own doctor first.

Locations (1)

VMR Institute for Vitreous Macula RetinaHuntington Beach, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06915922