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Keratoconus clinical trials

View clinical trials related to Keratoconus.

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NCT ID: NCT00642044 Recruiting - Keratoconus Clinical Trials

Corneal Collagen Crosslinking With Riboflavin for Keratoconus Treatment: A Brazilian Study

Start date: February 2007
Phase: N/A
Study type: Interventional

Cross-linking of the cornea increases the mechanical and biochemical stability of the stromal tissue. The purpose of this study is to assess the effectiveness of riboflavin-ultraviolet light induced cross-linking of corneal collagen in improving visual acuity and reducing progression of keratoconus in the Brazilian population.

NCT ID: NCT00626717 Completed - Keratoconus Clinical Trials

Riboflavin Mediated Corneal Crosslinking for Stabilizing Progression of Keratoconus

CCL
Start date: August 2007
Phase: Phase 2/Phase 3
Study type: Interventional

Background: Corneal cross linking is a procedure that induces collagen cross linking of the corneal stroma due to release of reactive oxygen radicals upon activation of topically applied riboflavine A by UVA exposure. This procedure might be capable of reducing keratocouns progression. Purpose: Although there are no randomised controlled trials on the effectiveness of corneal cross linking for the treatment of keratoconus it gains more and more importance in the general clinical setting. Therefore, the investigators started such randomised, placebo controlled, double blinded, multicenter trial to find out if this treatment is as effective as it promises to be. Methods: Randomised, placebo controlled, double blinded, multicenter trial.

NCT ID: NCT00593190 Completed - Clinical trials for Hydrops in Keratoconus

Intracameral Gas SF6 (Sulfur Hexafluoride) Injection for Acute Hydrops in Keratoconus

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

Intracameral Gas SF6 (Sulfur Hexafluoride) Injection for Acute Hydrops in Keratoconus

NCT ID: NCT00584285 Completed - Keratoconus Clinical Trials

Corneal Topographer Fluorescein Patterns

Start date: September 15, 2007
Phase:
Study type: Observational

The objective of this study is to determine if corneal topography can be used to predict the fluorescein pattern of keratoconus lenses on the eye. A corneal topography image will be taken and the computer selected lens will be placed on the eye. After placement of the lens color photographs will be taken of the eye's fluorescein pattern and compared to the computer predicted pattern.

NCT ID: NCT00567671 Completed - Corneal Ectasia Clinical Trials

Corneal Collagen Cross-Linking for the Treatment of Progressive Keratoconus and Corneal Ectasia

CL
Start date: December 2007
Phase: Phase 2/Phase 3
Study type: Interventional

Prospective, randomized, single site study to determine the safety and effectiveness of performing corneal collagen cross-linking (CCCL)using riboflavin and UVA light in eyes with corneal ectasia or progressive keratoconus.

NCT ID: NCT00566605 Active, not recruiting - Keratoconus Clinical Trials

Outcomes in a Comparison of Manual Penetrating Keratoplasty and the IntraLase® Enabled Keratoplasty

Start date: August 2007
Phase: Phase 1
Study type: Interventional

To compare the early visual results and postoperative recovery between two groups of keratoconic patients - one group having undergone a traditional, mechanical vacuum trephine procedure while the second group underwent femtosecond-enabled penetrating keratoplasty.

NCT ID: NCT00560651 Recruiting - Keratoconus Clinical Trials

German Corneal Cross Linking Register

Start date: November 2007
Phase:
Study type: Observational

Corneal Cross Linking is new treatment modality for patients with keratoconus. A keratoconus is characterized by progressive bulging and thinning of the eye's cornea. Keratoconus is a potentially severely sight impairing condition that may necessitate corneal transplantation in the progressive state. Corneal Cross Linking is designed to - increase the cornea's mechanical stability - to stop progression of bulging and thinning of the cornea - to prevent the need for corneal transplantation Corneal Cross Linking is performed by 1. Applying Riboflavin (Vitamin B2) eye drops every 2 minutes for 30 minutes to the cornea 2. Illuminating the cornea with UV-light This register of Corneal Cross Linking procedures performed in Germany serves to - gather long-term results - detect rare complications and side-effects - evaluate the efficacy in a large number of patients

NCT ID: NCT00435799 Recruiting - Keratoconus Clinical Trials

Evaluating Collagen Cross-Linking (CCL) Treatment in Norway

Start date: February 2007
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to assess safety, efficacy and stability of riboflavin-UV induced cross-linking of corneal collagen in reducing the progression of keratecatasia and in improving visual acuity. This is the first Norwegian study concerning CCL.

NCT ID: NCT00409955 Completed - Keratoconus Clinical Trials

Lamellar Transplant With Lyophilized Corneas

Start date: December 2005
Phase: Phase 2
Study type: Interventional

- The goals of this study are to develop a lyophilization method for anterior lamellar transplants in Brasil and to make a comparative analysis among patients transplanted with lyophilized and optisol corneas

NCT ID: NCT00384501 Terminated - Keratoconus Clinical Trials

Management of Patients With Keratoconus With Intacs

Start date: January 2000
Phase: N/A
Study type: Interventional

Purpose To evaluate long-term follow up of Intacs microthin prescription inserts (Addition Technology Inc, Fremont, Calif) for the management of keratoconus. Design A long-term (five years) retrospective, follow-up study