Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Abbott Medical Optics
Age
22–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Minimum 22 years of age
Bilateral cataracts
Preoperative keratometric cylinder in both eyes
Most appropriate toric IOL model choice (ZCT300 or ZCT400)
Predicted residual refractive cylinder, based on the AMO Toric IOL Calculator, must be:
≤ 0.69 D for a ZCT300 IOL or ≤ 0.88 D for a ZCT400 IOL
Clear intraocular media other than cataract in each eye
Availability, willingness, ability and sufficient cognitive awareness to comply with examination procedures and study visits
Ability to understand, read and write English in order to consent to study participation and complete a study questionnaire
Signed informed consent and HIPAA authorization
You may not be if
Irregular corneal astigmatism
Any corneal pathology/abnormality other than regular corneal astigmatism
Previous corneal surgery
Recent ocular trauma or intraocular surgery that is not resolved/stable or may affect visual outcomes
Any pupil abnormalities
Subjects with conditions associated with increased risk of zonular rupture, including capsular or zonular abnormalities that may lead to IOL decentration, including pseudoexfoliation, trauma, or posterior capsule defects
Known ocular disease or pathology that may affect visual acuity or that may require surgical intervention during the course of the study
Concurrent participation or participation during 30 days prior to preoperative visit in any other clinical study
Planned monovision correction
Patient is pregnant, plans to become pregnant, is lactating or has another condition associated with the fluctuation of hormones that could lead to refractive changes
