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Binocular Custom Vision Utilizing The Light Adjustable Lens (LAL)

NCT04533191 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 25

Last updated 2024-05-20

No results posted yet for this study

Summary

The objective of this investigator initiated study (IIT-001) is to obtain data on clinical methods which can be used during the examination of patients desiring binocular custom vision with the Light Adjustable Lens (LAL). An analysis of the collected data will be performed to determine whether these clinical assessments can be used by doctors to enhance their patient's clinical outcome.

Conditions

  • Cataract
  • Pseudophakia

Interventions

PROCEDURE

LAL IOL lens

Standard of care Cataract surgery with IOL placement

Sponsors & Collaborators

  • Vance Thompson Vision

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
110 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-09-01
Primary Completion
2021-01-01
Completion
2021-02-01
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT04533191 on ClinicalTrials.gov