Surgical Outcomes After Routine Cataract Extraction & Implantation of a Conventional or Spheric Intraocular Lens

Not Applicable

Completed

• Conditions: Cataract Extraction

• Registration Number: NCT00366496
• Lead Sponsor: Medical University of South Carolina

Brief Summary

To determine quality of vision post cataract extraction and intraocular lens (IOL) implantation of 2 different acrylic intraocular lenses: Acrysof® Single-Piece IOL and Acrysof® WF, through evaluation of contrast sensitivity, glare testing, visual outcomes, wavefront, corneal topography, and patient satisfaction.

Detailed Description

Not available

Study Timeline

• Study Start: 2004-07
• Study Completion: 2005-05
• Status Verified: 2005-07
• Study First Submitted: 2006-08-17
• Study First Submitted QC: 2006-08-17
• Last Update Submitted: 2006-08-17
• Study First Posted: 2006-08-21
• Last Update Posted: 2006-08-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Unilateral or bilateral cataract
• Eligible for phacoemulsification with primary implantation of a posterior chamber IOL. If bilateral, patient will receive the same IOL than the fellow eye.
• Expected maximum of 4 weeks and minimum of 1 week interval between primary and second eye surgeries when bilateral.
• Best corrected visual acuity (BCVA) should be no better than 20/40 in the presence of a glare source using Snellen visual acuity. In the Snellen visual acuity chart, better than 20/40 will be at least 3 letters read correctly in the 20/30 line.
• Naturally dilated pupil (in dim light) ≥ 4.0 mm in both eyes.

Exclusion Criteria

• Preoperative ocular pathology potentially affecting visual acuity
• Previous intraocular or corneal surgery.
• Keratometric astigmatism exceeding 1.5 diopters.
• Planned postoperative refraction for mono-vision.
• Current contact lens usage.
• Other ocular surgery at the time of the cataract extraction.
• Uncontrolled diabetes.
• Any neurological condition that might interfere with performance of required test.
• Auto-immune deficiency disease.
• Other severe acute or chronic medical or psychiatric condition that may increase the risk associated with study participation or study device implantation or may interfere with the interpretation of study results.
• Use of any systemic or topical drug known to interfere with visual performance.

Surgical Exclusion Criteria

• Significant anterior chamber bleeding.
• Detached Descemet's membrane
• Iris damage
• Posterior capsule rupture
• Radial tear in capsulorhexis
• Vitreous loss
• Zonular rupture.
• Use of corneal sutures for more than 1 week.

Post-implantation Exclusion Criteria

• Haptic not in the capsular bag.
• Descentration of the IOL of more than 1.0 mm
• Ocular pathologies potentially affecting visual acuity that were not evident prior to surgery.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Contrast sensitivity
Visual acuity

Secondary Outcome Measures

Name	Time	Method
Induction of hight order aberrations
Corneal topography
Patient satisfaction