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A Study Assessing Safety and Efficacy of MD-15 Intraocular Lens in Patients With Aphakic Eye After Cataract Surgery

Phase 3
Completed
Conditions
Cataract
Interventions
Device: MD-15 Intraocular Lens
Registration Number
NCT02888210
Lead Sponsor
Santen Pharmaceutical Co., Ltd.
Brief Summary

To evaluate safety and efficacy of MD-15 intraocular lens implanted into the aphakic eyes

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
110
Inclusion Criteria
  • Patients who intend to undergo phacoemulsification cataract extraction
Exclusion Criteria
  • Patients who undergo secondary implantation
  • Patients with vision loss induced by causes other than cataract
  • Patients who the principal investigator/subinvestigator considers ineligible for enrollment

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
MD-15MD-15 Intraocular LensInvestigational intraocular lens
Primary Outcome Measures
NameTimeMethod
Corrected visual acuityWeek 52
Secondary Outcome Measures
NameTimeMethod
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