RecruitingCataract
A Prospective, Randomized, Subject and Vision-assessor Masked, Multicenter Study Comparing Bilateral Clareon PanOptix, Bilateral Clareon PanOptix Pro, and Mixed Clareon PanOptix Pro/Vivity Intraocular Lens Implantation in Cataract Subjects
Eligible age
40+ yrs
Accepts
All genders
Locations
2 states
Healthy volunteers
Yes
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
Prospective, randomized, multicenter, multi-arm, subject and vision-assessor-masked, two stage study with Stage 1 as a three-arm initial enrollment period, followed by Stage 2 as a head-to-head study refined based on the Stage 1 data.
Sponsor: Berkeley Eye Center
You may qualify if…
- ✓ Adult cataract patients aged 40 years and older scheduled for age related cataract surgery in both eyes.
- ✓ Ability to understand and sign an ethics committee-approved informed consent form.
- ✓ Willingness and ability to attend all scheduled study visits as required by the protocol.
- ✓ Postoperative potential visual acuity of 20/25 or better in each eye, as determined by the investigator.
- ✓ Preoperative corneal astigmatism that can be corrected with a T3 or T4 toric IOL, or with a spherical IOL and LRIs or AKs resulting in a predicted postoperative astigmatism of less than 0.5 diopters (D).
- ✓ Ability to understand and complete questionnaires.
You may not qualify if…
- ✕ Women who are pregnant, planning to become pregnant during the study, or breastfeeding.
- ✕ Ocular conditions that could confound study results, including moderate to severe corneal pathology, irregular astigmatism, moderate to severe dry eye, preexisting retinal diseases such as macular degeneration or diabetic retinopathy.
- ✕ Any form of confirmed glaucomatous damage (ie, mild, moderate, or severe glaucoma).
- ✕ Participation in another clinical study that could interfere with the results.
- ✕ Systemic conditions that may affect healing or visual outcomes (e.g., uncontrolled diabetes mellitus, certain autoimmune disorders).
- ✕ Subjects with nystagmus, strabismus, zonular laxity or dehiscence, and pseudoexfoliation.
- ✕ Prior ocular surgery (except for uncomplicated cataract surgery in the fellow eye).
- ✕ Participants desiring monovision.
Where it's recruiting
Pennsylvania
Plymouth Meeting
Texas
Houston
Source: ClinicalTrials.gov · NCT06922084 · last updated 2025-04-10