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Clinical study of customized aspherical intraocular lens implants

Clinical study of customized aspherical intraocular lens implants

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONRC-12002154
Enrollment
Unknown
Registered
2012-04-08
Start date
2011-04-30
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Age-related cataract

Interventions

Experimental group:The experimental group was undergone Pentacam corneal spherical aberration measurement before surgery
the targeted range for residual total spherical aberration after surgery was set to 0 - 0.3 um
randomly assigned group:Randomly assigned patients were randomly implanted with an AO lens or a Tecnis ZA9003 lens.

Sponsors

Liexi Jia
Lead Sponsor

Eligibility

Sex/Gender
All
Age
51 Years to 84 Years

Inclusion criteria

Inclusion criteria: The selection criteria were as follows: aged between 50 and 85 years old and diagnosed with only age-related cataracts; pre-surgical axial range: 22 - 26 mm; normal cognition; normal tear film; the ability to attend follow-ups as scheduled.

Exclusion criteria

Exclusion criteria: The exclusion criteria were as follows: previous history of impaired visual recovery after surgery, including pre-surgical eye trauma, retinal diseases, glaucoma and corneal disease; history of corneal refractive surgery; post-surgical complications, including increased intraocular pressure and endophthalmitis.

Design outcomes

Primary

MeasureTime frame
post-surgical total spherical aberration;Contrast and glare sensitivities three months after surgery;

Secondary

MeasureTime frame
Pre- and post-surgical corneal spherical aberration;Post-surgical LogMAR vision;

Countries

China

Contacts

Public ContactLiexi Jia
jialiexi@163.com+86 13901074337

Outcome results

None listed

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