Actively Recruiting
HUD Surgical Guidance for Toric Alignment
Led by Gainesville Eye Associates · Updated on 2026-01-08
100
Participants Needed
1
Research Sites
51 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
HUD Surgical Guidance for Toric Alignment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients undergoing uncomplicated cataract surgery with toric IOL implantation
- Eyes implanted with a toric intraocular lens (IOL)
You will not qualify if you...
- Ocular conditions likely to impair vision after surgery
- History of eye trauma or instability of eye support structures
- Previous refractive eye surgery
- Irregular corneal astigmatism or keratoconus
- Physical or intellectual disabilities affecting eye fixation or understanding (e.g., Down's Syndrome, Parkinson's Disease)
- Unreliable eye measurement results
- Severe dry eye or other eye surface diseases
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
North Georgia Eye Associates
Gainesville, Georgia, United States, 30501
Actively Recruiting
Research Team
D
Dr. Clayton Blehm Blehm, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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