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

This trial accepts healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

  • Intraoperative aberrometer

    Device

    the patient intraocular lens will be optimized during the aphakic period after cataract extraction and before intraocular lens implantation, this will produce a possible change in the dioptric power of the intraocular lens

  • Preoperative intraocular lens calculation

    Other intervention

    the intraocular lens in this group will be calculated preoperatively with Barrett Universal II formula

Treatment groups

300 Participants
are divided into 2 treatment groups
Group A: ORA groupExperimental treatment 1 intervention
Group B: Control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

spherical equivalent

Spherical equivalent values at 90 days of the postoperative period

Time frame
90 days of the postoperative period

Secondary outcomes

1

uncorrected distance visual acuity

uncorrected distance visual acuity at 90 days of the postoperative period

Time frame
90 days of the postoperative period

Other outcomes

Sponsors and contacts

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