Evaluating the Need for the Pseudophakic Intraoperative Abberrometry in Toric IOL Implantation
Status: | Completed |
---|---|
Conditions: | Ocular, Ocular |
Therapuetic Areas: | Ophthalmology |
Healthy: | No |
Age Range: | 30 - Any |
Updated: | 1/31/2019 |
Start Date: | March 19, 2018 |
End Date: | January 14, 2019 |
Evaluating the Need for Pseudophakic Intraoperative Abberrometry in Toric IOL Implantation
To determine clinically significant difference in results obtained from cataract surgery
using IA. One eye will receive aphakic measurements only and the fellow eye will receive
aphakic and then pseudophakic measurements when implanting a toric IOL.
using IA. One eye will receive aphakic measurements only and the fellow eye will receive
aphakic and then pseudophakic measurements when implanting a toric IOL.
To determine if there is a clinically significant difference in the results obtained for the
toric IOL implantation when using IA to measure the aphakic eye only and when using IA to
measure the aphakic eye and then the pseudophakic eye, with toric IOL implantation.
toric IOL implantation when using IA to measure the aphakic eye only and when using IA to
measure the aphakic eye and then the pseudophakic eye, with toric IOL implantation.
Inclusion Criteria:
- willing and able to understand and sign an informed consent
- willing and able to attend all study visits
- presenting for uncomplicated bilateral cataract surgery and have an interest in a
toric iol
- have good ocular health, with no pathology that compromises visual acuity (outside of
residual refractive error)
- have visually significant cataracts
- have regular corneal astigmatism of 1.0D to 5.0D in both eyes with a difference
between eyes of 1.0D or less
- have potential post operative acuity of 20/25 or better
Exclusion Criteria:
- corneal pathology
- amblyopia
- prior corneal refractive surgery or other refractive surgery
- previous anterior or posterior chamber surgery that the investigator feels may
compromise visual outcomes
- Diabetic retinopathy if the investigator feels this will compromise visual outcomes
- macular degeneration
- history of retinal detachment
- irregular astigmatism or keratoconus
- strabismus
- if in the surgeon's opinion the subject is not an appropriate candidate for iol
implantation
- subjects who have an acute or chronic disease or illness that would confound the
results of this investigation
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