Keratoconus, Artificial Intelligence, Support Vector Machine Clinical Trial
Official title:
Efficiency of an Algorithm Derived From Corneal Tomography Parameters to Distinguish Highly Susceptible Corneas to Ectasia From Healthy
Verified date | March 2020 |
Source | Sao Jose do Rio Preto Medical School |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The objective of this study was to identify and build an algorithm through an imaging process using a support vector machine (SVM) with the tomography variables of cases with, KC, highly susceptible corneas to ectasia (HSCE), and healthy corneas and to compare this algorithm to BAD-D (Belin_Ambrosio Display) and PRFI (Pentacam Random Forest Index). The study included 148 eyes with KC, 351 with healthy corneas, and 88 eyes with HSCE.
Status | Completed |
Enrollment | 588 |
Est. completion date | January 1, 2018 |
Est. primary completion date | January 1, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: Patients were considered to be very asymmetric (VAE-NT) if the diagnosis of ectasia was confirmed in one eye based on the previously described criteria and the fellow eye had a normal front surface curvature (topometric) map. Objective criteria for considering normal topography was applied for defining the cases of VAE-NT, including objective front surface curvature metrics derived from Pentacam. Normal topography was rigorously considered based on objective criteria (27, 28) of a maximum curvature Kmax (Steepest Front Keratometry) <47.2 diopters, a paracentral inferior-superior (I-S value) asymmetry value at 6 mm (3-mm radii) < 1.45, and keratoconus percentage index (KISA%) score < 60 and (29). The cutoff point used to discriminate normal corneas and VAE-NT from KC corneas was the maximal posterior elevation (< 29 µm). This cutoff point had been determined in a previous study, using the same instrument and the same setting. The posterior elevation map was displayed with a 5-mm color-coded scale, and maximal posterior elevation was measured manually using the cursor in the central 5 mm. Exclusion Criteria: The following exclusion criteria were adopted: history of ocular trauma; chronic use of eye medication, glaucoma; dry eye syndrome; corneal scarring; neurotrophic keratopathy; severe meibomian gland dysfunction; vulnerable state owing to physical or mental illness and with language-related difficulties; pregnant or breastfeeding. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Gildasio Castello de Almeida Junior | Fundação de Amparo à Pesquisa do Estado de São Paulo |
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* Note: There are 12 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
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Primary | CTMVI designed to screen patients prior to refractive surgery | ROC curves of CTMVI comparing with BAD D, and PRFI | january 2012 until january 2018 |