Prospective study of AcuFocus IC-8 intraocular lens

Prospective study of AcuFocus IC-8 intraocular lens - Prospective study of IC-8

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000027518

Enrollment

Registered

2017-06-01

Start date

2017-05-15

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

Implantation of IC-8 intraocular lens

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patient have visual disturbances due to cataract. 2. Patient well understands the explanation of the study by doctor.

Exclusion criteria

Exclusion criteria: 1. Recurrent anterior/posterior ocular inflammation, pupil dislocation 2. Previous history of retinal hole, proliferative diabetic retinopathy, macular diseases and retinal detachment 3. Glaucoma with poor IOP control 5. Under pregnancy, lactating, intraoperative complication including continuous intraocular bleeding, vitreous prolapse and posterior capsule rupture)

Design outcomes

Primary

Measure	Time frame
Uncorrected visual acuity at 3 month after surgery(far, intermediate, near)	—

Secondary

Measure	Time frame
Best corrected visual acuity at 3 month after surgery (far, intermediate, near)	—

Countries

Japan

Contacts

Public ContactJunko Sawada

Nagoya Eye Clinic General affairs department

sawada@lasik.jp0120758049

Outcome results

None listed

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