N/A
N=71
Rotational Stability of the AcrySof® Toric
Cataract
Bottom Line
View on ClinicalTrials.gov: NCT00762216 ↗Enrolled (actual)
71
Serious AEs
0.0%
Results posted
May 2010
Primary outcome: Primary: Rotational Stability — 4 degrees
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- AcrySof® Toric intraocular lens (Device)
- Age
- Adult, Older Adult · 40+ yrs
- Sex
- All
- Sponsor
- Alcon Research
- Primary completion
- Jun 2009
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Rotational Stability |
4 | — |
| SECONDARY Residual Refractive Cylinder |
0.4 | — |
Summary
To assess the rotational stability and the residual refractive cylinder and patient reported outcomes of the AcrySof Toric intraocular lens after unilateral or bilateral implantation.
Eligibility Criteria
Inclusion Criteria
- Monolateral or bilateral cataracts
- anticipated intraocular lens (IOL) power of +10 Diopters (D) ~ +25D
- 0.75 ~ 2.0 D of astigmatism measured preoperatively by Keratometry readings
- able to sign the informed consent, to comply with scheduled visits and other study procedures
Exclusion Criteria
- Preoperative ocular pathology
- previous intraocular or corneal surgery
- an increased risk for complications which could require vitreoretinal surgery
- corneal irregularities
- corneal opacities
- current contact lens usage
- uncontrolled diabetes
Data sourced from ClinicalTrials.gov (NCT00762216). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.