Clinical outcomes after new monofocal intraocular lens with extended depth of focus(Eyhance) implantations

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0005713

Enrollment

Registered

2020-12-29

Start date

2020-05-26

Completion date

Unknown

Last updated

2021-01-06

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

Conditions

None listed

Interventions

Medical Device : As single group intervention model, extended-depth-of-focus intraocular lenses were implanted binocularly during cataract surgery.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: adults with significant bilateral immature cataract, less than 1.0 D corneal astigmatism, and potential acuity meter visual acuity greater than 0.1 logMAR

Exclusion criteria

Exclusion criteria: subjects who had undergone previous ocular surgery or trauma, had corneal opacity, retinopathy, glaucoma, uveitis, or amblyopia, or experienced complications such as posterior capsule rupture during the surgery.

Design outcomes

Primary

Measure	Time frame
Uncorrected monocular distance visual acuity;Uncorrected binocular distance visual acuity;Uncorrected intermediate visual acuity;Uncorrected near visual acuity;corrected monocular distance visual acuity;corrected binocular distance visual acuity;autorefraction;monocular and binocular defocus curves;contrast sensitivity;satisfaction questionnaire	—

Secondary

Measure	Time frame
Intraocular pressure	—

Countries

Korea, Republic of

Contacts

Public ContactHungwon Tchah

Asan Medical Center

Outcome results