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Synergy Lens Outcomes Evaluation

NCT05418153 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 52

Last updated 2024-03-18

Study results available
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Summary

This is a single visit study to evaluate the visual outcomes and patient satisfaction of patients who were bilaterally implanted with the Tecnis Synergy IOL between June 1 and December 31, 2021 in 2 centers in USA

Conditions

Interventions

DEVICE

Tecnis Synergy IOL

Intraocular lens replaces the natural lens removed during cataract surgery in both eyes.

Sponsors & Collaborators

  • Science in Vision

    collaborator OTHER

  • Center For Sight

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-03-14
Primary Completion
2022-11-22
Completion
2022-11-22
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05418153 on ClinicalTrials.gov