Evaluation of Glistenings in Intraocular Lenses Implanted in Normal Patients Following Routine Cataract Extraction.

Withdrawn before enrolling · Phase 4

Conditions studied: Glistenings

In brief

Evaluation of glistenings in intraocular lenses implanted in normal patients following routine cataract surgery. The lenses used will be Model X-60 made by the AVS company Vs AcrySof MA50BM made by the Alcon company.

Key facts

Study ID

NCT01131481

Run by

Fry Eye Associates and Fry Eye Surgery Center

People needed

0

Starts

2010-06-01

Expected to finish

2013-07-01

Last updated by the study team

2015-09-15

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18 years or older
• Bilateral cataracts requiring surgery
• Potential visual acuity of 20/40 or better in both eyes
• Require IOL power in range of 15-25 diopters
• Pupillary dilation of at least 6mm
• Willing and able to provide informed consent and attend follow-up appointments to 3 years

You may not qualify if…

• Any co-existing ocular disease or previous ocular surgery that would confound findings in the study, especially those effecting quality of vision. Examples include Macular degeneration amblyopia and prior epiretinal membrane peel.

Where it is running

• Fry Eye Associates — Garden City, Kansas, United States

Full record on ClinicalTrials.gov

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