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A Clinical Study on Improving the Accuracy of Intraocular Lens Power Calculation for the Second Eye Based on the Refractive Error of the First Eye in Cataract Patients with Prior Myopic Corneal Refractive Surgery.

A Clinical Study on Improving the Accuracy of Intraocular Lens Power Calculation for the Second Eye Based on the Refractive Error of the First Eye in Cataract Patients with Prior Myopic Corneal Refractive Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128547
Enrollment
Unknown
Registered
2026-07-22
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Age-related cataract, high myopia complicated cataract

Interventions

Cataract surgery group of both eyes after corneal refractive surgery:None

Sponsors

Wenzhou Medical University Affiliated Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 to 80 years old, gender not limited; 2. Have a history of LASIK/PRK surgery in both eyes (at least 3 months after the operation), and both eyes have been diagnosed with cataracts simultaneously or successively through ophthalmic examination, and have successively undergone phacoemulsification aspiration combined with intraocular lens implantation for cataracts in both eyes; 3. Standardized eye examinations were completed both before and after the operation, and there was at least one standardized subjective refraction within 1 week to 6 months after the operation. The clinical data are complete. 4. The Best Corrected Visual Acuity (BCVA) after the operation was less than 0.52logMAR;

Exclusion criteria

Exclusion criteria: 1. There are already ophthalmic lesions that may affect the postoperative optometry results before cataract surgery (including but not limited to corneal abnormalities, glaucoma, strabismus, suspensive ligament abnormalities, uveitis and severe retinopathy, ocular trauma), and a history of ocular surgery (such as retinal surgery, posterior scleral reinforcement surgery); 2. Severe complications occur during cataract surgery (such as posterior capsular rupture, lens nucleus detachment into the vitreous cavity, and severe damage to the corneal endothelium); 3. Combined with other serious ocular diseases (such as active endophthalmitis, severe corneal scarring);

Design outcomes

Primary

MeasureTime frame
PE of the second eye;

Secondary

MeasureTime frame
Preoperative ocular parameters: AL,K1,K2,ACD,LT;The type of IOL actually implanted during the operation and the diopter;The equivalent spherical diopter (SE) and best corrected visual acuity (BCVA) of both eyes after surgery;

Countries

China

Contacts

Public ContactPan Anpeng

Wenzhou Medical University Affiliated Eye Hospital

pananpeng@126.com+86 15005778161

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026