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

Open Label, Phase/3 Study Assessing Safety and Efficacy of MD-15 Intraocular Lens in Patients With Aphakic Eye After Cataract Surgery

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02888210
Enrollment
110
Registered
2016-09-02
Start date
2016-09-03
Completion date
2017-11-22
Last updated
2018-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cataract

Brief summary

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

Interventions

DEVICEMD-15 Intraocular Lens

Sponsors

Santen Pharmaceutical Co., Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Corrected visual acuityWeek 52

Countries

Japan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026