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Performance of Extended Depth of Focus (EDOF) multifocal SCL for intraocular lens implanted eyes

Evaluation of performance of Extended Depth of Focus (EDOF) soft contact lens for intraocular lens implanted eyes - EDOF SCL for IOL implanted eyes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs032200118
Enrollment
17
Registered
2020-09-14
Start date
2020-10-10
Completion date
Unknown
Last updated
2025-07-18

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

Conditions

IOL implanted eyes after cataract surgery

Interventions

Sponsors

Takahiro Hiraoka
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: -Men and women who understand the contents of the consent explanation document and their informed consents can be obtained. -Those whose ages are between 20 and 75 -Those who had undergone cataract surgery 1 month ago or before -Those who have monofocal or toric intraocular lenses inserted in both eyes -Those have spherical equivalent from 0.00 to -6.00D by refraction test -Those who require near or far vision correction -Those who have a total astigmatism of 1.00D or less in both eyes by refraction test -Those who have corrected distance vision in both eyes of 0.7 or better (decimal visual acuity)

Exclusion criteria

Exclusion criteria: - Patients with moderate or severe grade of corneal/conjunctival or eyelid abnormalities - Patients with uveitis - Patients with dry eye and lacrimal disease that are problematic for lens wear - Patients with allergic diseases that can affect lens wear - Patients with diabetics - Patients with a history of anaphylaxis - Patients with serious cardiac, hepatic, renal, pulmonary, hematological disorders and other complications that are considered inappropriate for the study. - Patients who have participated in other trials within the last 3 months - Pregnant women, women who are breastfeeding or plan to become pregnant during the study - Patients who used hard contact lens (including Orthokeratology lens) within the last 1 month - Patients who wear contact lenses in 1 eye only. - Patients who are judged to be ineligible for the study by the investigators and those are considered unsuitable for wearing soft contact lenses by the investigators.

Design outcomes

Primary

MeasureTime frame
Visual acuity at various distances at contrast sensitivity of 100%

Secondary

MeasureTime frame
- Visual acuity at various distances at contrast sensitivity of 40% and 20% - Visual acuity at far and near in open filed - Contrast sensitivity with stripe vision chart - Stereopsis

Contacts

Public ContactHiraoka Takahiro

University of Tsukuba Hospital

thiraoka@md.tsukuba.ac.jp+81-29-853-3148

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Feb 4, 2026