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Clinical trials of FineVision (PhysIOL) trifocal intraocular lens

Clinical trials of FineVision (PhysIOL) trifocal intraocular lens - FineVision

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000024869
Enrollment
50
Registered
2016-11-18
Start date
2015-12-15
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 causing impaired visual function

Interventions

FineVision(Micro F), FineVision(Pod F), FineVision(Toric)

Sponsors

Kanazawa Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who are expected to achieve improved visual function by cataract surgery within the range of IOL diopters.

Exclusion criteria

Exclusion criteria: Patients with a history of ocular diseases including: age-related macular degeneration of the macula; advanced glaucoma (severe visual field abnormality); keratoconus; ruptured Zinn's zonule and other corneal diseases. Patients with a history of cornea refractive surgery and patients excluded by a responsible doctor for other reasons to be stated.

Design outcomes

Primary

MeasureTime frame
Visual acuity (VA; non-corrected VA, corrected VA, contrast VA, functional VA, near distance VA, etc.)is measured the next day after surgery, one week, one month, three months, six months, one year, then every year.

Secondary

MeasureTime frame
refraction, accommodative power, form of anterior ocular segment, corneal endothelium, corneal form, corneal thickness, pupil diameter, forward light scattering, backward light scattering, higher-order aberrations, retinal image contrast, diagnosis of anterior ocular segment by slit-lamp microscopy, measurement of anterior chamber protein content

Countries

Japan

Contacts

Public ContactSasaki Hiroshi

Kanazawa Medical University Department of Ophthalmology

ophthal@kanazawa-med.ac.jp076-286-2211

Outcome results

None listed

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