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Study Evaluating Visual Outcomes in Post-Myopic LASIK Patients After Implantation of the Odyssey Intraocular Lens

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Healthy Volunteers: f
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⁃ Subjects MUST fulfill the following conditions to qualify for enrollment into the trial

• Age: 50 years and older.

• Gender: Males and Females.

• Bilateral cataracts

• Bilateral implantation of Odyssey IOLs (toric and non-toric)

• Scheduled to undergo standard cataract surgery in both eyes, within 1 to 30 days between surgeries.

• Willing and able to provide written informed consent for participation in the study.

• Willing and able to comply with scheduled visits and study examination procedures.

• Postoperative best corrected visual acuity of 0.2 logMAR (20/32 Snellen) or better in each eye.

Locations
United States
Florida
Center For Sight
RECRUITING
Venice
Contact Information
Primary
Helga P Sandoval
hps@cepmd.com
8438813937
Time Frame
Start Date: 2025-08-18
Estimated Completion Date: 2026-08-18
Participants
Target number of participants: 30
Treatments
Other: Odyssey IOL
Related Therapeutic Areas
Sponsors
Leads: Center For Sight
Collaborators: Sengi Clinical

This content was sourced from clinicaltrials.gov