Odyssey Evaluation in Post LASIK Patients

Part of paid clinical trials in Venice, Florida.

Sponsor
Center For Sight
Study ID
NCT07260695
Phase
PHASE4
Status
Recruiting
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Conditions

  • Cataract

Eligibility Criteria

Sex
ALL
Age
50 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Odyssey intraocular lens — DEVICE
    The Odyssey intraocular lens is intended to be implanted at the time of cataract surgery to replace the natural lens.

Study Details

This prospective study evaluates the visual and refractive outcomes of the TECNIS Odyssey intraocular lens (IOL) implanted in patients with a history of myopic LASIK. Given the unique optical challenges of post-LASIK eyes, including altered corneal curvature and higher-order aberrations, the study aims to assess the IOL's performance in terms of distance, intermediate, and near vision, and patient satisfaction. Its design features may offer favorable outcomes in these patients.

Key Dates

Start date
Aug 18, 2025
Status verified
Dec 2025
Primary completion
Aug 18, 2026
Completion
Aug 18, 2026

Study Design

Enrollment
30 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Other: Odyssey IOL

Primary Outcome Measure

Binocular defocus curve [ Time Frame: 3 months postoperatively ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Center For SightVeniceFlorida34285
Gina Thomas
[email protected]
941-263-4784

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By research site
Center For Sight· Venice, FL

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