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Intraoperative Aberrometry vs Conventional Intraocular Lens Calculation, a Prospective Study.

RecruitingNAAges 40 Years - anyAllInstituto de Oftalmología Fundación Conde de Vale…
NCT06219252 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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

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📋 Eligibility rules (as published)
Inclusion Criteria: * patients with senile cataract, patients undergoing phacoemulsification, complete biometric profile, axial length calculated by interferometer. Exclusion Criteria: * glaucoma, uncontrolled diabetic retinopathy, pseudoexfoliation syndrome, aged macular degeneration , dry eye syndrome, other ocular pathologies.
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What it tests

  • Intraoperative aberrometer
  • Preoperative intraocular lens calculation
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Where

1 site
Instituto de oftalmología Fundación Conde de Valenciana
Mexico City, Mexico
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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