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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40+
SponsorInstituto de Oftalmología Fundación Conde de Valenciana

About this trial

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

Eligibility criteria

Qualifiers

patients with senile cataract, patients undergoing phacoemulsification, complete biometric profile, axial length calculated by interferometer.

Disqualifiers

glaucoma, uncontrolled diabetic retinopathy, pseudoexfoliation syndrome, aged macular degeneration , dry eye syndrome, other ocular pathologies.

Trial design

Treatments tested in this trial

  • Intraoperative aberrometer
  • Preoperative intraocular lens calculation

Treatment groups

300 Participants
are divided into 2 treatment groups