Actively Recruiting
This Clinical Trial Compares Two Phacoemulsification Systems Used in a Bilateral Cataract Surgery Subjects in Order to Study CDE and Ultrasound Time During Cataract Removal
Led by Nicole Fram M.D. · Updated on 2026-03-18
30
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This clinical trial compares two phacoemulsification systems used in a bilateral cataract surgery subjects, in order to study CDE and Ultrasound time during cataract removal
CONDITIONS
Official Title
This Clinical Trial Compares Two Phacoemulsification Systems Used in a Bilateral Cataract Surgery Subjects in Order to Study CDE and Ultrasound Time During Cataract Removal
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy patients 18 years or older undergoing uncomplicated sequential bilateral cataract surgery with phacoemulsification and intraocular lens implantation
- Expected to have cataract surgery in both eyes
- Both eyes must have nuclear sclerosis cataracts graded 3 or above using LOCS III
- Both eyes will be operated on by the same surgeon
- Ability to provide informed consent for the study and planned procedure
You will not qualify if you...
- Patients under 18 years of age
- Complex cataract cases involving zonulopathy or requiring zonular support devices
- Need for mechanical pupil expanding devices during surgery
- Undergoing femtosecond laser-assisted lens fragmentation
- Surgical complications judged to interfere with outcomes
- Prior ocular surgery within 3 months or any surgery interfering with outcomes
- Presence of endothelial cell dystrophies or corneal comorbidities
- History of intraocular inflammation such as uveitis or iritis
- History of retinal edema or significant epiretinal membrane
- History of retinal surgery involving vitrectomy
- Dense brunescent cataract judged to interfere with outcomes
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Advanced Vision Care
Los Angeles, California, United States, 90067
Actively Recruiting
Research Team
O
Orly Shiler
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
2
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