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MD-15 Intraocular Lens Phase 3 study

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

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1080224664
Enrollment
110
Registered
2019-05-07
Start date
2016-09-03
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Cataract

Interventions

investigational material(s) Generic name etc : MD-15 (Intraocular lens) INN of investigational material : - Therapeutic category code : --- Other Dosage and Administration for Investigational material

Sponsors

Santen pharmaceutical co.,ltd
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who intend to undergo phacoemulsification cataract extraction

Exclusion criteria

Exclusion criteria: - Patients who undergo secondary implantation - Patients with vision loss induced by causes other than cataract - Patients who have been deemed ineligible as participants in the study by investigator/subinvestigator

Design outcomes

Primary

MeasureTime frame
efficacy Visual acuity after surgery

Secondary

MeasureTime frame
safety efficacy Visual acuity, adverse events, etc.

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026