Implantable contact lens (ICL) to correct myopia, are safe, effective and have predictable results for correcting moderate to high myopia or nearsightedness. These are the conclusions discussed in an article published in the September issue of Ophthalmology, the clinical journal of the American Academy of Ophthalmology.
The article provided an update to the U.S. Food and Drug Administration’s long-term, follow-up multi-center STAAR Myopic Implantable Contact Lens (ICL) clinical investigation. The STAAR ICL is one of the lenses expected to receive FDA approval. A competing ICL, the Verisyse lens, to be sold by AMO Inc., has received approval by the FDA’s device panel and is also expected to receive FDA approval at about the same time.
For the study, the STAAR myopic ICL was implanted in 526 eyes of nearly 294 patients whose myopia ranged from -3.0 to -20.0 diopters. The lens was inserted through a tiny incision and placed in front of the eye’s natural lens. The study found that at three years, nearly 60 percent of the patients had 20/20 or better visual acuity and nearly 95 percent had 20/40 or better. Reports of symptoms such as glare halos, double vision, night vision and difficulty driving at night either decreased or remained unchanged. Ninety seven percent of the patients said they would chose ICL implantation again. Less than one percent of the patients said they were dissatisfied.
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