At a glance
ClinicalIndex Comparison RecordN/ACompleted· 104 enrolled
Drug / intervention
Acrylic IOL +2 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.
Corrected VA With Long-Term Follow-Up After AcrySof® IOL Implantation
In Brief
A clinical study evaluating Acrylic IOL, Silicone IOL, and 1 other intervention for Pseudophakia. Completed, enrolled 104 participants.
Detailed Summary
The purpose of this study is to compare the long-term visual acuity (VA) with an acrylic IOL to a silicone or polymethylmethacrylate (PMMA) IOL in cataract patients. This study will take place in Japan.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPseudophakia
Countries--
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedMay 2015
Enrollment StartJun 2015
Primary CompletionMay 2016
TodayJul 2026
First PostedMay 21, 2015
Enrollment StartJun 1, 2015
Primary CompletionMay 1, 2016
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 11.1 years ago
Interventions
Acrylic IOLdevice
Acrylic IOL for long-term implantation in the cataract patient
Silicone IOLdevice
Silicone IOL for long-term implantation in the cataract patient
PMMA IOLdevice
Polymethylmethacrylate IOL for long-term implantation in the cataract patient