A study of visual function in 5-year postoperative patients with the multifocal posterior chamber lens LENTIS Comfort

A study of visual function in 5-year postoperative patients with the multifocal posterior chamber lens LENTIS Comfort LS-313 MF15 - A study of visual function in 5-year postoperative patients with the multifocal posterior chamber lens LENTIS Comfort LS-313 MF15

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000048353

Enrollment

Registered

2022-07-21

Start date

2022-07-01

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

Patients after cataract surgery

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who participated in the clinical trial and were 5 years post-LC implantation

Exclusion criteria

Exclusion criteria: Patients with complications (eye or systemic) that affect postoperative visual function not related to LC implantation

Design outcomes

Primary

Measure	Time frame
Visual acuity	—

Countries

Japan

Contacts

Public ContactTsuyoshi Yoshimura

Santen Pharmaceutical Co., Ltd. Japan Medical Affairs

clinical@santen.co.jp06-4802-9337

Outcome results