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Keratoconus clinical trials

View clinical trials related to Keratoconus.

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NCT ID: NCT03531047 Completed - Keratoconus Clinical Trials

Refractive Corneal Cross-linking for Progressive Keratoconus

Start date: November 1, 2018
Phase: N/A
Study type: Interventional

Young patients with keratoconus face two problems: disease progression and corneal shape irregularity. Both underlie the 20% rate of corneal transplantation in keratoconics required to maintain useful vision. Corneal collagen cross-linking (CXL) is a now the gold-standard treatment to halt disease progression. The aim is to strengthen the cornea to prevent further shape deterioration. For patients whose quality of vision has already suffered, standard CXL can generally only prevent further deterioration, rather than improving vision. Refractive CXL, a new iteration of CXL in which a bespoke treatment pattern is applied to the cornea, aims to smooth out surface irregularities thereby improving vision. This primary objective of this study is to compare the visual outcome in patients with progressive keratoconus treated with refractive CXL, as compared with historical controls treated with standard CXL.

NCT ID: NCT03511495 Completed - Keratoconus Clinical Trials

Reliability of Topography Measurements in Keratoconus

Start date: September 11, 2017
Phase:
Study type: Observational

The purpose of this study is to assess the reliability and repeatability of the parameters obtained using the Galilei dual-scheimpflug corneal topographer for monitoring progression in eyes with keratoconus.

NCT ID: NCT03504800 Recruiting - Keratoconus Clinical Trials

OCT in Diagnosis of Irregular Corneas

Start date: May 1, 2018
Phase:
Study type: Observational

This main goal of this study is to improve the detection, classification, monitoring, and treatment of irregular corneas due to keratoconus, warpage, dry eye, scar, stromal dystrophies, and other corneal conditions. The primary goal will be achieved by using optical coherence tomography (OCT) to: 1. Develop an OCT-based system to classify and evaluate corneal-shape irregularities. 2. Develop OCT metrics for more sensitive detection of keratoconus progression. 3. Develop OCT-and-topography guided phototherapeutic keratectomy (PTK) for irregular corneas.

NCT ID: NCT03462355 Completed - Keratoconus Clinical Trials

Tobacco Smoking Among Crosslinked-keratoconus Patients

TOBACOLINK
Start date: March 1, 2014
Phase: N/A
Study type: Observational

Certain studies reported that cigarette by-products may make the cornea more rigid, suggesting that it could lead to "natural" CXL of collagen fibers, hence a protective effect for KC. Others have reported that cigarette smoking causes no significant changes in the corneal biomechanics. The aim of this study was to assess a possible link between keratoconus (KC) occurrence and patients' smoking habits.

NCT ID: NCT03450213 Not yet recruiting - Keratoconus Clinical Trials

Astigmatism in Keratoconus Patients

Start date: October 1, 2019
Phase: N/A
Study type: Interventional

Keratoconus is a bilateral (but usually asymmetrical) non-inflammatory progressive thinning process of the cornea. It manifests as characteristic cone-like ectasia of the cornea associated with irregular stromal thinning, resulting in a cone-like bulge , which causing irregular astigmatism and vision impairment.

NCT ID: NCT03442751 Completed - Clinical trials for Progressive Keratoconus

Study to Evaluate the Safety and Efficacy of Epi-on Corneal Cross-linking in Eyes With Progressive Keratoconus

Start date: April 6, 2018
Phase: Phase 3
Study type: Interventional

To evaluate the safety and efficacy of epithelium-on corneal collagen cross-linking (CXL) in impeding the progression of, and/or reducing corneal curvature (Kmax) in eyes with progressive keratoconus. Epithelium-on CXL uses a formulation that allows the riboflavin to penetrate the cornea without the need to remove the epithelium, the outer most layer of the cornea.

NCT ID: NCT03429569 Recruiting - Keratoconus Clinical Trials

Cross-Linking ACcéléré Iontophorèse Confocal kératocONE

CLACICONE
Start date: August 12, 2015
Phase: Phase 4
Study type: Interventional

A monocentric, parallel-arm, prospective, randomized therapeutic trial that compares the efficacy of two curative keratoconus treatment techniques by cross-linking collagen (accelerated conventional technique or iontophoresis). The primary endpoint will be the depth of the demarcation line measured by confocal microscopy and OCT at 1 month. This line represents the limit depth between treated and untreated stroma.

NCT ID: NCT03355430 Completed - Clinical trials for Moderate Keratoconus

Simultaneous Corneal Wavefront-Guided Trans-PRK and Corneal Collagen Crosslinking After ICRS Implantation for Moderate Keratoconus

Start date: July 7, 2016
Phase: N/A
Study type: Observational

The investigators aim to investigate the effects of combined corneal wavefront-guided transepithelial photorefractive keratectomy (tPRK) and accelerated corneal collagen cross-linking (CXL) after intracorneal ring segment (ICRS) implantation in patients with moderate keratoconus. Medical records of 23 eyes of 23 patients undergoing combined tPRK and CXL after ICRS implantation were retrospectively analyzed. Uncorrected distance visual acuity (UDVA), corrected distance visual acuity (CDVA), manifest refraction spherical equivalent (MRSE), corneal indices based on Scheimpflug tomography, higher-order aberrations (HOAs), and corneal biomechanical properties were evaluated before and after ICRS implantation, and at 1, 3, and 6 months after combined tPRK and CXL. Corneal biomechanical properties were measured using the dynamic Scheimpflug analyzer at approximately the same time of day.

NCT ID: NCT03288116 Completed - Keratoconus Clinical Trials

Objective and Subjective Diagnostic Parameters in the Fellow Eye of Unilateral Keratoconus

Start date: January 2, 2014
Phase: N/A
Study type: Observational

patients with keratoconus in one eye and forme fruste keratoconus in the fellow eye compared to normal subjects .the patients were examined by schemipflug imaging system (Pentacam)

NCT ID: NCT03249233 Recruiting - Keratoconus Clinical Trials

Corneal Thickness Changes With Scleral Contact Lenses

Start date: June 22, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate changes in the corneal thickness of scleral contact lens wearers in a keratoconic (KC) population and compare to age-matched controls. The hypothesis is that scleral contact lens wear is associated with low levels of corneal hypoxia including measurable changes in corneal thickness. Corneal thickness will be altered post scleral lens wear compared to pre-lens wear and the amount of alteration will correlate to the fitting characteristics in the central zone of the scleral lenses. We propose to take a sample of keratoconic and control participants, fit them in scleral lenses, and to measure topographic corneal thickness after 8-10 hours of scleral lens wear after three weeks of wear, to compare two instruments in the measurement of corneal thickness, and to compare the effects of varying central corneal clearance of the scleral lens on corneal thickness.