New lens aims to match top cataract implant in vision quality
NCT ID NCT07571694
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares a new domestic trifocal lens (D615L) to the Zeiss AT LISA tri 839MP for people having cataract surgery. 90 adults with age-related cataracts will receive one of the two lenses and be followed for 6 months to measure vision at different distances. The goal is to see if the new lens is as good or better than the established one.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- trifocal intraocular lens (D615L)
- What this could lead to
- If successful, this could show that the new D615L lens provides similar or better vision at all distances after cataract surgery, offering a more affordable option.
- What could go wrong
- This is a small, early-stage study with only 90 participants, so results may not apply to everyone. The new lens might not perform as well as the established Zeiss lens.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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90 people
The number who actually took part.
- Started
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Apr 2025
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
patients with age-related cataract
- Ages
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50 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * diagnosed age-related cataract; * preoperative corneal astigmatism \<1.0 D; * endothelial cell count \>2000/mm²; * signed informed consent and ability to complete 6-month follow-up Exclusion Criteria: * prior corneal refractive, glaucoma or vitreoretinal surgery; * intraoperative posterior capsule rupture, zonular dehiscence or vitreous loss; * corneal pathology, macular edema or optic neuropathy affecting visual assessment; * active ocular inflammation, glaucoma, maculopathy or diabetic retinopathy; * uncontrolled systemic disease such as diabetes or autoimmune disorders.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Shanghai Tenth People's Hospital
Shanghai, Shanghai Municipality, 200000, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- A simple blood draw might reveal hidden eye lymphoma
- Can a new lens make glasses obsolete after cataract surgery?
- Can a new lens design sharpen vision after macular surgery?