Skip to content

Real-world study of PRL for refractive correction in patients with high myopia

Real-world study of PRL for refractive correction in patients with high myopia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043600
Enrollment
Unknown
Registered
2021-02-23
Start date
2021-02-22
Completion date
Unknown
Last updated
2021-06-14

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

Conditions

High Myopia

Interventions

Single arm Experimental group :NA

Sponsors

Eye Hospital and School of Ophthalmology and Optometry, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Aged 20 to 50 years old; 2. Preoperative spherical lens power: -10.0D to -30.0D (including -10.0D and -30.0D); 3. Knowing and agreeing to participate in the Hundred People Bright Eyes Charity Action; 4. The posterior chamber intraocular lens (PRL) has been implanted in one or both eyes.

Exclusion criteria

Exclusion criteria: 1. Except for posterior chamber intraocular lens implantation in phakic eyes, the included eyes have a history of any other ocular trauma or surgery; 2. Corneal and other ocular diseases that affect vision (such as corneal opacity, keratitis, glaucoma, uveitis, lens dislocation or subluxation, lens laxative pocket, retinopathy, etc.); 3. Accompanied by severe or unstable heart, liver, kidney, lung, endocrine (including thyroid dysfunction), blood, mental nerve dysfunction and other diseases that affect the results of this study; patients with weakness or disease;

Design outcomes

Primary

MeasureTime frame
Best Corrected Visual Acuity;

Secondary

MeasureTime frame
Uncorrected Visual Acuity;Corneal endothelial cell loss;Vault;Intraocular Pressure;Spherical equivalent;Operation time;Complication;

Countries

China

Contacts

Public ContactA-Yong Yu

Eye Hospital and School of Ophthalmology and Optometry, Wenzhou Medical University

yaybetter@hotmail.com+86 13868760001

Outcome results

None listed

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