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RECRUITINGINTERVENTIONAL

Occyo Tele-ophthalmology Study

Evaluation of Diagnostic Effectiveness and Reliability of a Telemedical Examination with Occyo One Vs Traditional Slit Lamp-based Examination After Cataract Surgery

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The prospective, (observer) blinded clinical trial at the University Hospital for Ophthalmology includes patients routinely scheduled for cataract surgery at the Medical University of Innsbruck. Patients are enrolled one week prior to their planned cataract surgery. The participants will undergo a screening in which, in addition to the ophthalmological standard examinations, Occyo One images of the anterior segment of the eye are taken. After surgery, a post-operative follow-up visit takes place and a second set of Occyo One images will be generated. During the postoperative check-up, the study team at the trial center decides-based on defined criteria (medical history, slit lamp examination results)-whether a change in the subsequent patient management is necessary due to the presence of postoperative complications (unexpected management changes = UMC). Up on completion of all patient visits/study-specific measurements and data collection, information regarding diagnostic criteria and the Occyo One images are sent to an external, blinded ophthalmologist for telemedical assessment. Based on the available information and images, the blinded ophthalmologist decides whether a change in patient management should have been made or not. The difference in the detection of an event resulting in a UMC is the primary objective of this clinical investigation.

Who May Be Eligible (Plain English)

Who May Qualify: 1. Understands and agrees to comply with the study procedures and provides written willing to sign a consent form as documented by signature 2. Patients scheduled to undergo cataract surgery 3. Male or female patient aged ≥ 50 years at time of consent Who Should NOT Join This Trial: 1\. Woman of childbearing potential (WOCBP) Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: 1. Understands and agrees to comply with the study procedures and provides written informed consent as documented by signature 2. Patients scheduled to undergo cataract surgery 3. Male or female patient aged ≥ 50 years at time of consent Exclusion Criteria: 1\. Woman of childbearing potential (WOCBP)

Treatments Being Tested

DEVICE

Ocular surface imaging

Telemedical examination of high-resolution, all-in-focus images of the cornea, sclera, conjunctiva, and lid margins for montioring of postoperative complications

Locations (1)

Medical University Innsbruck, University Hospital for Ophthalmology and Optometry
Innsbruck, Austria