Actively Recruiting
Outcomes of Clareon PanOptix Pro in Patients With Prior Myopic Refractive Surgery
Led by Juliette Eye Institute Research Center · Updated on 2025-12-12
40
Participants Needed
1
Research Sites
96 weeks
Total Duration
On this page
Sponsors
J
Juliette Eye Institute Research Center
Lead Sponsor
S
Sengi
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study is a Single center, single arm, prospective, observational study of clinical outcomes following bilateral cataract surgery and Clareon PanOptix Pro implantation. Subjects will be assessed preoperatively, and at 1 and 3 months postoperatively. Clinical evaluations will include administration of the QUVID and IOLSAT questionnaires, manifest refraction, topography, as well as measurement of visual acuities at distance, intermediate, and near.
CONDITIONS
Official Title
Outcomes of Clareon PanOptix Pro in Patients With Prior Myopic Refractive Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults 45 years or older with confirmed age-related cataracts eligible for bilateral cataract surgery
- Prior binocular myopic photorefractive keratectomy (PRK) or myopic LASIK
- Regular corneal astigmatism less than or equal to 0.6 diopters and candidates for PanOptix Pro spherical IOL
- Patients with regular corneal astigmatism who are candidates for PanOptix Pro toric IOL T3
- Postoperative visual potential of monocular 20/25 or better as judged by the surgeon
You will not qualify if you...
- Any ocular condition that could impair postoperative visual acuity including corneal abnormalities, moderate to severe dry eyes not relieved by treatment, eye inflammation, retinal pathology, or glaucoma
- Pregnancy or lactation
- Any ocular surgery other than corneal myopic refractive surgery (LASIK or PRK)
- Physical or intellectual disabilities affecting fixation (e.g., Down's Syndrome, Parkinson's Disease)
- Apple Kappa/chord mu greater than or equal to 0.6
- Higher order corneal aberrations above specified thresholds at 4mm pupil diameter
- Requirement for a limbal relaxing incision
- Investigator discretion based on medical evidence indicating unsuitability for the trial
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Juliette Eye Institute Research Center
Albuquerque, New Mexico, United States, 87113
Actively Recruiting
Research Team
Z
Zoe Baker, OD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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