A Comparative Pilot Study Of High-Order Aberrations With Aspheric IOL Models SN60WF and ZCB00
Completed · Not applicable
Conditions studied: Cataracts
In brief
The purpose of this study was to prospectively compare high-order aberrations between eyes implanted with the AcrySof® Natural IQ (SN60WF) intraocular lens (IOL) versus those implanted with the Tecnis ZCB00 IOL.
Key facts
- Study ID
- NCT01105585
- Run by
- Alcon Research
- People needed
- 20
- Starts
- 2010-04-01
- Last updated by the study team
- 2012-11-29
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Requires bilateral extraction of cataracts by phacoemulsification followed by implantation of a posterior chamber intraocular lens;
- Confirmed absence of pre-existing conditions that could skew the results or present contraindications for the IQ intraocular lens (IOL) or the Tecnis ZCB00 IOL;
- <1 diopter corneal astigmatism preoperatively;
- Able to achieve 6.5 mm dilated pupil;
- Other protocol-defined inclusion criteria may apply.
You may not qualify if…
- Chronic disease or illness;
- Irregular optical aberration;
- Amblyopia;
- History of corneal disease (e.g., herpes simplex, herpes zoster keratitis, etc.);
- Diabetic retinopathy;
- Macular degeneration;
- History of retinal detachment;
- Other surgeries planned at time of cataract removal;
- Severe dry eye;
- Other protocol-defined exclusion criteria may apply.
Where it is running
- Contact Alcon Call Center for Trial Locations — Fort Worth, Texas, United States
Full record on ClinicalTrials.gov
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