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Study identifier: NCT07325188 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

HUD Surgical Guidance for Toric Alignment

Condition: Cataract and IOL Surgery  ·  Sponsor: Gainesville Eye Associates

PhaseNA
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Dr. Clayton Blehm Blehm, MD  ·  (770) 532-4444  ·  claytonblehm@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

North Georgia Eye AssociatesGainesville, Georgia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07325188