Actively Recruiting
Intraoperative Aberrometry vs Conventional Intraocular Lens Calculation, a Prospective Study.
Led by Instituto de Oftalmología Fundación Conde de Valenciana · Updated on 2025-05-14
300
Participants Needed
1
Research Sites
164 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
the goal of this intervention study is to compare prospectively the accuracy of the power calculation between both groups, the intraoperative aberrometry (ORA) vs barrett universal II preoperative calculation (control group) . Researchers will compare ORA group vs control to see changes in spherical equivalent and uncorrected distance visual acuity
CONDITIONS
Official Title
Intraoperative Aberrometry vs Conventional Intraocular Lens Calculation, a Prospective Study.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with senile cataract
- Patients undergoing phacoemulsification surgery
- Complete biometric profile available
- Axial length measured by interferometer
You will not qualify if you...
- Diagnosis of glaucoma
- Uncontrolled diabetic retinopathy
- Pseudoexfoliation syndrome
- Age-related macular degeneration
- Dry eye syndrome
- Other ocular pathologies
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Instituto de oftalmología Fundación Conde de Valenciana
Mexico City, Cuauhtemoc, Mexico, 06800
Actively Recruiting
Research Team
D
DIEGO ZAMORA - DE LA CRUZ, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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