New lens implant shows promise for clearer vision at all distances
NCT ID NCT06979557
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at how well the Odyssey intraocular lens works for people having refractive lens exchange to improve vision. Forty adults aged 40 and older received the lens in both eyes. Researchers measured vision at different distances and asked about symptoms and glasses use at least two months after surgery. The goal was to see if the lens provides good vision without major visual disturbances.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Odyssey intraocular lens (IOL) device
- What this could lead to
- If successful, this lens could improve near, intermediate, and distance vision after lens replacement surgery, reducing the need for glasses.
- What could go wrong
- This is a small, single-center study with only 40 participants and no comparison group. Results may not apply to everyone, and long-term effects are not assessed.
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
-
40 people
The number who actually took part.
- Started
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Jul 2025
- Finished
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Jan 2026
- 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
Eligible test subjects will be aged 40 years and older who underwent bilateral implantation with the Odyssey IOL.
- Ages
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40 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: * Participants will include 40 patients aged 40 years and older who have a measurable Potential Acuity Meter (PAM) of 20/20 electing to undergo bilateral refractive lensectomy surgery with IOL implantation. Exclusion Criteria: * Patients with significant ocular comorbidities (e.g., macular degeneration, glaucoma) or prior intraocular surgery will be excluded.
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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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Mann Eye Institute
Houston, Texas, 76134-2099, United States
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