At a glance
ClinicalIndex Comparison RecordPhase 3Completed· 250 enrolled
Drug / intervention
modified light transmission intraocular lens +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Clinical Evaluation of a Modified Light Transmission IOL
In Brief
A Phase 3 clinical trial evaluating modified light transmission intraocular lens and monofocal acrylic intraocular lens for Cataract. Completed, enrolled 250 participants across 11 sites.
Detailed Summary
The purpose of this study is to evaluate the safety and effectiveness of a new investigational modified light transmission monofocal intraocular lens compared to a conventional intraocular lens (IOL).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCataract
CountriesUnited States
Collaborators--
Timeline
Phase 3CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartDec 2006
First PostedSep 2008
Primary CompletionMar 2009
Study CompletionJun 2009
TodayJul 2026
First PostedSep 5, 2008
Enrollment StartDec 1, 2006
Primary CompletionMar 1, 2009
Study CompletionJun 1, 2009
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 17.8 years ago
Interventions
modified light transmission intraocular lensdevice
violet visible light blocking acrylic intraocular lens
monofocal acrylic intraocular lensdevice
conventional hydrophobic acrylic intraocular lens