Skip to content

A clinical study for trifocal intraocular lens implantation for presbyopia after cataract surgery

Visual function study for trifocal intraocular lens implantation after cataract surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900022519
Enrollment
Unknown
Registered
2019-04-15
Start date
2017-07-01
Completion date
Unknown
Last updated
2019-04-23

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

Conditions

cataract

Interventions

1:trifocal IOL implation
2:regional refractive IOL implantation
3:monofocal IOL implantation

Sponsors

Xi'an Fourth Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) cataract patients, including age-related cataract and complicated cataract without fundus disease; 2) corneal astigmatism<1.5D; 3) ocular axis<29mm; 4) clear cognitive ability; 5) corneal higher-order aberration <0.3 µm.

Exclusion criteria

Exclusion criteria: 1) corneal diseases, such as corneal degeneration, keratitis, corneal leukoma; 2) optic nerve diseases, such as glaucoma, ischemic optic neuropathy; 3) retinal diseases, such as retinal vascular disease, retinal detachment, macular degeneration; 4) lens subluxation; 5) previous history of trauma of eyes, excimer laser surgery or other intraocular surgery; 6) severe systemic diseases that cannot receive surgery.

Design outcomes

Primary

MeasureTime frame
visual acuity;modulation transfer function cutoff frequency;object scatter index;Strehl ratio;

Secondary

MeasureTime frame
patient satisfaction;spectacle independence;

Countries

China

Contacts

Public ContactMeifang Chu
2567437874@qq.com+86 18602948320

Outcome results

None listed

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