TerminatedInterventionalPhase 4Updated Oct 22, 2012
Investigation of Corneal Aberrations and Visual Outcomes in Patients Implanted With an AcrySof Toric Intraocular Lens (IOL) | NCT00878839 | Trialant
WithdrawnInterventionalNot ApplicableUpdated Aug 2, 2012
Investigation of Corneal Aberrations and Visual Outcomes in Patients Implanted With an AcrySof Toric Intraocular Lens (IOL)
ClinicalTrials.gov ID
NCT00878839
Lead Sponsor
Alcon ResearchINDUSTRY
Overall Status
Withdrawn
Study Type
Interventional
Phase
Not Applicable
Enrollment
0Actual
Last Update Posted
Aug 2, 2012Estimated
Start Date
Mar 2009
Primary Completion Date
Mar 2009Actual
Completion Date
Mar 2009Actual
Brief Summary
A prospective evaluation of postoperative corneal aberrations and visual parameters (e.g. visual acuity) in patients implanted with an AcrySof Toric IOL.
Cataracts
Astigmatism
Toric
Ages Eligible for Study
Adult (18-64)Older Adult (65+)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Operable cataracts;
Good ocular health;
Qualifies for AcrySof Toric IOL via AcrySof Toric Calculator (1.03-2.06 D cylinder at corneal plane)