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Comparing Monofocal IOLs in Highly Myopic Cataract Patients

W

Wenzhou Medical University

Status

Not yet enrolling

Conditions

Cataract

Treatments

Other: no intervention

Study type

Observational

Funder types

Other

Identifiers

NCT06905938
H2025-014-K-13

Details and patient eligibility

About

Comparison of Postoperative Outcomes in Patients with High Myopia Undergoing Cataract Surgery Implanted with Extended Depth of Focus Intraocular Lens (ICB00) and Monofocal Intraocular Lens (ZCB00)

Full description

In this study, we aim to compare the visual outcomes and quality of life between highly myopic patients with cataracts who receive implantation of extended depth of focus (EDOF) intraocular lenses (ICB00) and monofocal intraocular lenses (ZCB00). This is a case-control study, planning to recruit 64 highly myopic patients with cataracts, aged between 40 and 70, with 32 in each group. The primary endpoints of the study are the best-corrected visual acuity (BCVA) and defocus curve at 6 months postoperatively. Secondary endpoints include uncorrected visual acuity (UCVA), contrast sensitivity, intraocular pressure, and assessments of patient satisfaction and quality of life. These will be evaluated using standardized questionnaires such as the VF-14, the PRSIQ spectacle dependency scale, and reading speed tests to quantify changes in vision-related quality of life. Patients will undergo comprehensive ophthalmic examinations preoperatively and at 6 months postoperatively, including slit-lamp anterior segment examination, fundus examination, corneal topography, and intraocular pressure testing. Additionally, questionnaires will be used to assess patients' subjective satisfaction with visual improvement and spectacle needs in daily life. All data will be statistically analyzed to compare the effects of the two types of intraocular lenses. Continuous variables will be analyzed using t-tests or Mann-Whitney U tests, and categorical variables will be analyzed using chi-square tests. The level of statistical significance is set at p<0.05. Through this study, we hope to determine whether the use of EDOF intraocular lenses provides better visual outcomes and quality of life compared to monofocal intraocular lenses in highly myopic patients with cataracts. The results of this study will provide a more scientific basis for the choice of intraocular lenses in clinical practice.

Enrollment

60 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 1: The patients are between 40 and 70 years old.

    2: Ocular axis > 26mm

    3: Able to understand, cooperate and complete all follow-up.

Exclusion criteria

  • 1: Moderate and severe dry eye

    2: There is macular degeneration complicated by high myopia.

    3: Combined with other ophthalmic diseases

    4: Previous history of ophthalmic surgery.

    5: There are intraoperative or postoperative complications.

Trial design

60 participants in 2 patient groups

ICB00 implantation after cataract surgery.
Description:
Undergoing micro-incision cataract surgery with the implantation of an extended depth of focus (EDOF) intraocular lens (ICB).
Treatment:
Other: no intervention
ZCB00 implantation after cataract surgery.
Description:
Performing micro-incision cataract surgery and implanting a ZCB (presumably an abbreviation specific to a certain type of intraocular lens) intraocular lens
Treatment:
Other: no intervention

Trial contacts and locations

1

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Central trial contact

Zhao Yune; li siyan

Data sourced from clinicaltrials.gov

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