Clinical trial Recruiting at 1 site Observational Ages 18 to 100

Visual adaptation and quality of life after different IOL implantation options

Official title: Evaluation of Visual Adaptation and Optical Performance in Patients With Bilateral Multifocal or Mix-and-Match Intraocular Lens Implantation: A Longitudinal Observational Study

Run by Sichuan Academy of Medical Sciences · NCT07740590 · Data updated 2026-11-12

This study follows adults who have cataracts and receive bilateral multifocal or mixed IOLs to see how their vision and daily life improve over 6 months.

More Cataract trials

Quick facts

Study typeObservational
Ages18 Years to 100 Years
SexAll
Enrollment264 (estimated)
SponsorSichuan Academy of Medical Sciences
Academic / other
Locations1 site (Chengdu)
StatusRecruiting
StartedMarch 1, 2025
Main results expectedOctober 31, 2027
Study endsDecember 31, 2027
Registry record updatedJuly 31, 2026
Trial IDNCT07740590 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 and older with age-related cataract, scheduled for bilateral IOL implantation, with low corneal astigmatism and good overall health who are willing to complete follow-up.

Probably not a fit

Individuals with ocular comorbidities affecting vision, prior ocular surgery, or complications during/after surgery may not experience the same benefits.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective observational study examines long-term visual adaptation, optical quality, and patient-reported outcomes after bilateral implantation of multifocal or mix-and-match intraocular lenses. Participants are adults with age-related cataract undergoing bilateral phacoemulsification, followed at multiple postoperative time points from 1 week to 6 months. Standard ophthalmic tests and validated questionnaires, including the MMAQ, are used to track changes in visual performance, spectacle independence, and overall satisfaction. The study aims to describe trajectories of neuroadaptation to optical phenomena such as glare and halos in real-world conditions. Interventions are observational in nature, involving various bilateral IOL strategies, without randomization or assignment by the researchers.

Why it matters

Potential benefit: If successful, results could guide doctors in choosing IOL strategies that optimize patient satisfaction and visual function after cataract surgery.

How similar studies have gone: Previous research has shown variable neuroadaptation to multifocal IOLs; this study adds longitudinal data on adaptation trajectories with mix-and-match strategies.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 18 years or older with age-related cataract requiring bilateral phacoemulsification and intraocular lens (IOL) implantation
* Corneal astigmatism less than 0.75 D
* Good general health and willing to complete all postoperative follow-up visits
* Signed written informed consent

Exclusion Criteria:

* Previous ocular surgery or ocular trauma
* Coexisting ocular diseases affecting visual potential, such as corneal opacity, glaucoma, macular degeneration, or diabetic retinopathy
* Intraoperative or postoperative complications (e.g., posterior capsule rupture)
* Systemic diseases that may interfere with visual outcomes or follow-up compliance

Where it's running

  • Sichuan Provincial People's Hospital
    Chengdu, China
    Recruiting

Study contacts

  • Principal investigator: Chao Qu — School of Medicine, University of Electronic Science and Technology of China
  • Study coordinator: Xiangjun Fu, Ph.D.
  • Email: 243981469@qq.com
  • Phone: +86-28-87393999

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • Rotational Stability of the Acunex Vario Toric

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  • Anterior segment anatomy assessment with swept-source OCT in eye surgery patients

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  • MiLOOP-assisted cataract surgery for dense cataracts

    In people with dense cataracts, this study tests whether using the miLOOP device during cataract surgery can protect corneal cells and reduce ultrasound energy, compared with standard surgery.

    Recruiting Universiti Kebangsaan Malaysia Medical Centre · Cheras, Kuala Lumpur · NCT07898007

  • Corneal Biomechanics and Surgical Astigmatism after Cataract Surgery in Pseudoexfoliation

    This study tests how the cornea's biomechanical properties before cataract surgery relate to the amount of blinking surgically induced astigmatism, comparing people with pseudoexfoliation to those without.

    Recruiting Eye Clinic Medic Zuljan Jukic · Split, Splitsko-dalmatinska County · NCT07722247

  • Neuroplastic pain education and guided breathing during awake cataract surgery

    This trial tests whether the STEIN Protocol, a non-drug approach with pain education, guided imagery, and paced breathing, helps adults having cataract surgery require less pain medicine and feel less anxious.

    Recruiting University of California, Los Angeles · Los Angeles, California · NCT07715591

  • Bilateral Implantation of enVista Envy Trifocal IOL for Cataract Patients

    This study tests whether the enVista Envy trifocal intraocular lens can provide good distance, intermediate, and near vision after cataract surgery in adults who want less dependence on glasses.

    Recruiting Pomeranian Medical University Szczecin · Szczecin, Zachodnipomorskie · NCT07696130

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.