RECRUITING

RLE Outcomes With Bilateral Implantation of Odyssey 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

This study is a single center, ambispective study of visual outcomes after successful bilateral implantation of the Odyssey IOL. Subjects will be assessed at least 2 months postoperatively at a single visit. Clinical evaluations will include administration of the AIOLIS questionnaire, as well as measurement of visual acuities at distance, intermediate, and near, monocular (right eye) and binocular defocus curve, and refractive outcomes.

Official Title

Ambispective Analysis of Patient Reported Outcomes and Visual Acuity in Patients Undergoing a Refractive Lens Exchange With Bilateral Implantation Odyssey Intraocular Lenses

Quick Facts

Study Start:2025-05-31
Study Completion:2026-06-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06979557

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:40 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Participants will include 40 patients aged 40 years and older who have a measurable Potential Acuity Meter (PAM) of 20/20 electing to undergo bilateral refractive lensectomy surgery with IOL implantation.
  1. * Patients with significant ocular comorbidities (e.g., macular degeneration, glaucoma) or prior intraocular surgery will be excluded.

Contacts and Locations

Study Contact

Melissa Hamann Wright
CONTACT
832-368-0117
melissa.wright@manneye.com

Principal Investigator

Phillip Brunson, OD
PRINCIPAL_INVESTIGATOR
Mann Eye Institute

Study Locations (Sites)

Mann Eye Institute
Houston, Texas, 76134-2099
United States

Collaborators and Investigators

Sponsor: Mann Eye Institute

  • Phillip Brunson, OD, PRINCIPAL_INVESTIGATOR, Mann Eye Institute

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 Date2025-05-31
Study Completion Date2026-06-01

Study Record Updates

Study Start Date2025-05-31
Study Completion Date2026-06-01

Terms related to this study

Additional Relevant MeSH Terms

  • Refractive Lens Exchange