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Irregular; Contour of Cornea clinical trials

View clinical trials related to Irregular; Contour of Cornea.

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NCT ID: NCT05377515 Completed - Cataract Clinical Trials

Evaluation of Visual Outcomes in Patients With Complex Corneas Implanted With the IC-8 IOL

Start date: February 10, 2022
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to evaluate visual outcomes in patients with complex corneas who have been previously implanted with the IC-8 IOL after cataract removal.

NCT ID: NCT04570020 Recruiting - Keratoconus Clinical Trials

Scleral Lens Fitting Using Wide-Field OCT

Start date: September 23, 2020
Phase:
Study type: Observational

The purpose of this study is to see if OCT technology can optimize scleral contact lens fittings. Subjects with keratoconus, post-penetrating keratoplasty (PK), post-LASIK ectasia, post-radial keratotomy (RK), or a variety of anterior surface disorders requiring scleral lens fittings will be considered for enrollment. For each study eye, a clinically-selected scleral lens fit will be compared against an OCT-selected lens fit. The quality of each lens fit will be determined by flourescein exam at the slit lamp. Apical clearance, limbal clearance, conjunctival compression, and lens edge lift will be assessed. A lens that satisfies all four criteria will be considered satisfactory.

NCT ID: NCT03612284 Completed - Clinical trials for Irregular; Contour of Cornea

Scleral Contact Lens Insertion Solution Study

Start date: November 27, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the clinical ocular compatibility (feasibility of safety and efficacy) of a patented solution (US Patent 2,259,437, Stone) which contains multiple essential ions and has a pH and tonicity which more closely mimics human tears as compared to the subjects' current habitual scleral lens insertion solution.

NCT ID: NCT02444923 Completed - Keratoconus Clinical Trials

Scleral Versus Corneal RGP Contact Lenses in Irregular Cornea Disorders

Start date: October 25, 2015
Phase: N/A
Study type: Interventional

The most common causes for irregular cornea (IC) in hospital contact lens practice are Keratoconus (KC) and related cornea thinning disorders. These conditions cause mild to marked impairment of vision and cannot be effectively corrected by spectacles and soft contact lenses. The gold standard in the management of KC is Corneal Rigid Gas Permeable contact lenses (corneal lenses), which correct approximately 90% of the corneal irregularity. Compared with a normal cornea, the cornea in KC is irregular and this results in a compromise to the fit of rigid corneal lenses. Specifically, they bear on the cornea and this, together with the vulnerability of the cornea in KC, are implicated in corneal scarring, and disease progression as well as a significantly reduced vision related quality of life (QoL) in KC compared with corneal lens wearers who have no KC. In cases where the compromise fit of corneal lenses proves problematic, large diameter Scleral RGP contact lenses (scleral lenses) may be used as a problem solver. Unlike the smaller corneal lenses which bear on the cornea, the scleral lenses completely bridge over the cornea and bear on the sclera. The aim of this research is to investigate the performance of scleral lenses in KC participants who habitually wear corneal lenses. The research question: is there a measurable difference in the visual performance and visual quality of life in participants with Irregular cornea disorders like keratoconus and other related conditions, who habitually wear corneal lenses in comparison with scleral lenses.