Clinical Trials Directory

Trials / Completed

CompletedNCT01970267

Clear Vision Study

Randomized Trial of Laser Ablation for Highly Symptomatic Floaters

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
35 (actual)
Sponsor
University of British Columbia · Academic / Other
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

Vitreous floaters are tiny, cloudy, clumps of cells that appear in the otherwise clear fluid (vitreous) that fills the back 3/4 of the eye. Floaters are commonly caused by eye conditions such as posterior vitreous detachment (PVD), vitreous syneresis and asteroid hyalosis. While these symptoms are considered physiological in nature, they can be of considerable inconvenience to many patients which affect essential activities. The investigators wish to assess the safety and efficacy of floater treatment in patients with highly symptomatic floaters using an FDA approved nanosecond infrared yttrium aluminum garnet (YAG) lasers.

Conditions

Interventions

TypeNameDescription
PROCEDURELaser Ablation of Floaters
PROCEDURESham Laser TreatmentLaser will be set at 0.3 millijoules (mJ). There will be a 100% absorptive filter (black spot) of about 1cm placed centrally on the lens. All laser aiming beams will be placed within the 1cm filter. Laser will be applied at 0.3 mJ at the absorptive black spot (100% density filter) in order to create a realistic treatment therapy procedure.

Timeline

Start date
2013-10-01
Primary completion
2016-02-01
Completion
2016-02-01
First posted
2013-10-28
Last updated
2016-04-21

Locations

2 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT01970267. Inclusion in this directory is not an endorsement.