CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 40 enrolled
Drug / intervention
TECNIS Odyssey IOLdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06550375
NCT06550375N/ACompleted
CompareCT.gov

Ambispective Analysis of Patient Reported Outcomes and Visual Acuity in Patients With Bilateral Implantation of Odyssey Intraocular Lenses

Mann Eye Institute·observational·Posted Aug 13, 2024·Updated Apr 8, 2026

In Brief

An observational study evaluating TECNIS Odyssey IOL for Cataract. Completed, enrolled 40 participants across 1 site.

Detailed Summary

This study is a single center, ambispective study of visual outcomes after successful bilateral cataract surgery. Subjects will be assessed at least 3 months postoperatively at a single visit. Clinical evaluations will include administration of the AIOLIS and OSDI questionnaires, as well as measurement of visual acuities at distance, intermediate, and near.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsCataract
CountriesUnited States
CollaboratorsSengi

Timeline

N/ACompletedFinished
20252026
First PostedAug 13, 2024
Enrollment StartSep 5, 2024
Primary CompletionMar 26, 2025
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 1.9 years ago

Interventions

TECNIS Odyssey IOLdevice

Implantation with the TECNIS Odyssey IOL