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Keratoconus clinical trials

View clinical trials related to Keratoconus.

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NCT ID: NCT01143389 Completed - Keratoconus Clinical Trials

Corneal Crosslinking in Patients With Keratoconus and Post-Refractive Ectasia

Start date: May 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of using riboflavin and UV light to treat progressive keratoconus or post-refractive corneal ectasia.

NCT ID: NCT01069848 Completed - Keratoconus Clinical Trials

Feasibility Study of the Vedera KXS for Treatment of Keratoconus

Start date: January 2010
Phase: N/A
Study type: Interventional

The objective of this investigation is to evaluate the feasibility, safety and efficacy of the Vedera KXS for the reduction or elimination of myopia and astigmatism in patients with keratoconus, who are no longer able to achieve adequate vision with their contact lenses or glasses.

NCT ID: NCT00890266 Completed - Keratoconus Clinical Trials

Corneal Collagen Cross-linking With Hypotonic Riboflavin in Corneas Thinner Than 400 Microns

HypotonicRibo
Start date: April 22, 2009
Phase: N/A
Study type: Interventional

Corneal ectasia is a relative weakness in the structure of the cornea, which produces a progressive change in its shape which results in visual distortion. It is known that collagen cross-linking in the cornea occurs naturally with age, and in diabetes, both of which seem to prevent progressive ectasia. Corneal collagen cross-linking with riboflavin on corneas thicker than 400 microns has been shown to stabilize the cornea in keratoconus, and prevent progression of the disease. The purpose of this study is to determine whether corneal collagen cross-linking with riboflavin in a hypotonic solution, with UV light, on corneas less than 400 microns thick, leads to stabilisation of corneal ectasia.

NCT ID: NCT00887900 Completed - Keratoconus Clinical Trials

Deep Anterior Lamellar Keratoplasty (DALK)

DALK
Start date: January 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to report outcomes of deep anterior lamellar keratoplasty (DALK) using the big-bubble technique.

NCT ID: NCT00863876 Completed - Healthy Clinical Trials

Comparison of WaveLight Analyzer and Alcon LadarWave

Start date: March 2009
Phase: N/A
Study type: Observational

Comparison of repeated WaveLight Analyzer and Alcon LadarWave measurements in phakic and pseudophakic eyes.

NCT ID: NCT00850148 Completed - Keratoconus Clinical Trials

Comparison of Anwar and Melles Techniques in Deep Anterior Lamellar Keratoplasty (DALK) for Keratoconus Patients

Start date: May 2008
Phase: N/A
Study type: Interventional

This study will be performed on patients who come to labbafinejad ophthalmic clinic from 20 March 2008. Keratoconus diagnosis will be determined by clinical finding in slit lamp, keratometery and topographic characteristics. Patients will be randomly placed in group A and B. In group A, Anwar surgical method and in B, Melles surgical method, will be done. This is not a blind study due to surgeons' knowledge. All patients will receive Btamethazone drop and Chloramphenicol every 6 hours and will be tapered in two months. In the end anatomical results, complications, BCVA, UCVA, astigmatism, endothelial cell numbers will be compared in two groups by using specular microscopy. Contrast sensivity, central corneal diameter, interface wrinkling and opacity will be measured by metrovison, Confoscan, Photoslit in months 3, 6, 12, respectively and will be evaluated afterwards.

NCT ID: NCT00832897 Completed - Keratoconus Clinical Trials

Evaluation of Topical Riboflavin Exposed to UVA Radiation and Implantation of Corneal Ring

Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to postpone the corneal transplantation in keratoconus and promote the stiffness of the cornea across the riboflavin-UVA corneal collagen crosslinking , and after, corneal ring surgery.

NCT ID: NCT00802776 Completed - Keratoconus Clinical Trials

Femtosecond Laser Assisted Keratoplasty

FLAK
Start date: October 2007
Phase: N/A
Study type: Interventional

Penetrating keratoplasty (PKP) is corneal transplantation performed by using round trephine blades to create matched circumferential incisions in both the diseased cornea and the donor cornea. The donor tissue graft is then secured in place with sutures which are usually removed postoperatively.The primary surgical goals are the preservation of a clear graft and improvement of vision. Surgical outcomes are limited by donor-recipient junction mismatch, astigmatism, rejection, infection and wound dehiscence. The femtosecond laser is a focusable, infrared laser capable of cutting tissue at various depths and in a range of patterns, and is currently being used to create corneal lamellar flaps in LASIK surgery. The laser parameters can be adjusted for submicron precision in cutting desired diameters, depths and shapes in the cornea, with minimal collateral injury. This technology is now capable of creating full-thickness corneal trephinations with customized locking edges at the graft-host junction between the donor and recipient corneas in Femtosecond Laser-Assisted Keratoplasty (FLAK). This approach may allow for better wound junction of the donor and recipient corneas, which in turn may also significantly reduce astigmatism, improve wound healing and visual recovery. This pilot study will help us determine optimal femtosecond laser spot size, separation, fluence, and energy which result in the best graft-host fit. The specific aim is to investigate postoperative physiology and biomechanics after FLAK in human eyes.

NCT ID: NCT00777322 Completed - Keratoconus Clinical Trials

T-Cat Laser & Cross-linking for Keratoconus

T-Cat
Start date: October 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether excimer laser corneal surface ablation (T−Cat) can be safely combined with simultaneous corneal collagen cross−linking treatment to produce an improved and stable corneal profile in the treatment of keratoconus.

NCT ID: NCT00647699 Completed - Clinical trials for Progressive Keratoconus

Corneal Collagen Cross-linking for Progressive Keratoconus

CXL
Start date: December 2007
Phase: Phase 3
Study type: Interventional

Prospective, randomized multicenter study to determine the safety and effectiveness of performing cornea collagen cross-linking (CXL) using riboflavin and UVA light in eyes with progressive keratoconus.