Clareon PanOptix Pro vs. Clareon PanOptix - Study B
Launched by ALCON RESEARCH · May 2, 2024
Trial Information
Current as of August 11, 2025
Completed
Keywords
ClinConnect Summary
This clinical trial, called Clareon PanOptix Pro vs. Clareon PanOptix - Study B, is looking at two types of lenses used in cataract surgery. Specifically, it compares the Clareon™ PanOptix™ Pro Trifocal Intraocular Lens (IOL) to the Clareon™ PanOptix™ Trifocal IOL. The goal is to determine which lens is safer and more effective for patients who have lost their ability to focus clearly due to conditions like aphakia (a condition where the eye's natural lens is missing) and presbyopia (difficulty seeing close objects with age).
To be eligible for this study, participants must be planning to have cataract surgery on both eyes and should have a specific level of vision (with less than 1.00 diopter of astigmatism) in each eye. They also need to be able to attend all study visits and understand the study details. However, women who are pregnant, planning to become pregnant, or breastfeeding are not eligible, nor are those with certain eye conditions or who want a specific type of vision correction called monovision. Participants in this trial can expect to attend several visits to monitor their progress and results after receiving one of the lenses. This study is currently active but not recruiting new participants at this time.
Gender
ALL
Eligibility criteria
- Key Inclusion Criteria:
- • Understand and sign an ethics committee-approved informed consent form;
- • Willing and able to attend all scheduled study visits as required by the protocol;
- • Planned cataract surgery (both eyes);
- • Preoperative corneal astigmatism less that 1.00 diopter in each eye.
- • Other protocol-defined inclusion criteria may apply.
- Key Exclusion Criteria:
- • Women of childbearing potential if currently pregnant, intend to become pregnant during the study, or are breastfeeding;
- • Ocular conditions as specified in the protocol;
- • Subjects who desire monovision correction.
- • Other protocol-defined exclusion criteria may apply.
About Alcon Research
Alcon Research is a leading global company dedicated to advancing eye care through innovative research and development. As a subsidiary of Novartis, Alcon focuses on the development of cutting-edge products and therapies for vision correction and eye health, including surgical, pharmaceutical, and consumer eye care solutions. With a commitment to enhancing the quality of life for patients worldwide, Alcon Research conducts rigorous clinical trials to evaluate the safety and efficacy of its products, ensuring that they meet the highest standards of care. Through collaboration with healthcare professionals and institutions, Alcon remains at the forefront of ophthalmic advancements, driving progress in the field of vision science.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Houston, Texas, United States
Cincinnati, Ohio, United States
Torrance, California, United States
Kansas City, Missouri, United States
Charleston, South Carolina, United States
Salt Lake City, Utah, United States
Nashville, Tennessee, United States
Bloomfield Hills, Michigan, United States
Patients applied
Trial Officials
Principal Clinical Trial Lead
Study Director
Alcon Research, LLC
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported