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Visual Outcomes and Patient Satisfaction With Vivity IOL in Post Refractive Patients

NCT06064916 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2025-05-23

Study results available
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Summary

This is a non-interventional, prospective, observational study of the outcomes for post myopic refractive surgery patients following successful, uncomplicated cataract surgery with bilateral implantation of the Vivity IOL (DAT\*\*\*/CCWET\*).

Patients will be assessed for monocular and binocular distance, intermediate, and near vision.

Conditions

  • Pseudophakia

Interventions

DIAGNOSTIC_TEST

Visual Acuity

Monocular and binocular measurement of distance, intermediate, and near visual acuity

DIAGNOSTIC_TEST

Defocus Curve

Measurement of a defocus curve

OTHER

Intraocular Lens Satisfaction (IOLSAT) Questionnaire

Self-reported post-operative patient satisfaction with vision after surgery

OTHER

Quality of Vision After Surgery (QUVID) Questionnaire

Self-reported post-operative patient vision quality after surgery

OTHER

Visual Disturbance Questionnaire

Questionnaire of self-reported visual disturbances of patients

DIAGNOSTIC_TEST

Topography and Tomography

Topography and tomography measurements with Atlas, iTrace, and/or Pentacam

Sponsors & Collaborators

  • Berkeley Eye Center

    lead OTHER

Principal Investigators

  • Morgan Micheletti, MD · Berkeley Eye Center

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-07-25
Primary Completion
2024-12-11
Completion
2024-12-11
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 NCT06064916 on ClinicalTrials.gov