COMPLETED

Visual Performance With Clareon® Vivity® Intraocular Lenses (IOLs)

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this study is to generate clinical data to quantify the impact of residual astigmatism on the overall visual performance during distance, intermediate, and near viewing in patients implanted with Clareon Vivity IOLs.

Official Title

Evaluation of the Impact of Residual Astigmatism on the Visual Performance With Clareon Vivity

Quick Facts

Study Start:2025-04-10
Study Completion:2025-06-13
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06784063

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:22 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Able to understand and sign an Institution Review Board-approved informed consent form;
  2. * Willing and able to attend all scheduled study visits as required by the protocol;
  3. * Implanted with study IOLs in both eyes at least 4 months prior to study participation;
  4. * BCDVA of 0 logMAR or better in each eye.
  1. * Residual astigmatism greater than or equal to 1.00 D;
  2. * Clinically significant ocular conditions as specified in the protocol;
  3. * History of ocular surgeries other than limbal relaxing incisions
  4. * Other protocol-specified exclusion criteria may apply.

Contacts and Locations

Principal Investigator

Clinical Trial Lead, Surgical CRD
STUDY_DIRECTOR
Alcon Research, LLC

Study Locations (Sites)

Grosinger, Spigelman & Grey Eye Surgeons, P.C
Bloomfield Hills, Michigan, 48302
United States
Key-Whitman Eye Center
Dallas, Texas, 75243
United States
Berkeley Eye Center
Sugar Land, Texas, 77478
United States

Collaborators and Investigators

Sponsor: Alcon Research

  • Clinical Trial Lead, Surgical CRD, STUDY_DIRECTOR, Alcon Research, LLC

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-04-10
Study Completion Date2025-06-13

Study Record Updates

Study Start Date2025-04-10
Study Completion Date2025-06-13

Terms related to this study

Keywords Provided by Researchers

  • Cataract
  • IOL

Additional Relevant MeSH Terms

  • Astigmatism