HUD Surgical Guidance for Toric Alignment

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorGainesville Eye Associates

About this trial

This study aims to assess the accuracy of toric intraocular lens (IOL) alignment axes as calculated and displayed by a novel digital guidance system. In addition, it evaluates the time required to initiate surgical guidance and postoperative refractive astigmatism following toric IOL implantation.

This single-surgeon, single-site, prospective, non-invasive observational study evaluated the accuracy of toric IOL alignment axes calculated and displayed by the digital guidance system (Cassini Technologies, B.V.) in 100 eyes. The intraoperatively calculated alignment axes were compared to preoperative measurements to assess their accuracy (in degrees). Postoperative outcomes, including residual refractive astigmatism (diopters) and visual acuity (Snellen), were recorded at 1 month postoperatively.

Eligibility criteria

Qualifiers

Patients undergoing uncomplicated cataract surgery with toric IOL implantation,

Eyes implanted with a toric IOL.

Disqualifiers

Ocular comorbidity likely to impair postoperative visual acuities, or

History of ocular trauma or zonular instability, or

Previous refractive surgery, or

Irregular corneal astigmatism or keratoconus, or

Trial design

Treatments tested in this trial

  • Cassini Guidance

Treatment groups

100 Participants
are divided into 1 treatment group

Sponsors and collaborators