Clinical Trials Logo

Stevens-Johnson Syndrome clinical trials

View clinical trials related to Stevens-Johnson Syndrome.

Filter by:

NCT ID: NCT02319616 Withdrawn - Clinical trials for Toxic Epidermal Necrolysis

Topical Clobetasol for the Treatment of Toxic Epidermal Necrolysis

TEN
Start date: November 2016
Phase: Phase 1/Phase 2
Study type: Interventional

The primary objectives of this study are to investigate the efficacy and safety of topical steroid ointment (clobetasol 0.05%) for the treatment of the cutaneous manifestations of toxic epidermal necrolysis (TEN).

NCT ID: NCT02149732 Available - Clinical trials for Limbal Stem Cell Deficiency

Clinical Trial on the Effect of Autologous Oral Mucosal Epithelial Sheet Transplantation

Start date: May 2014
Phase: Phase 1/Phase 2
Study type: Expanded Access

To investigate the effect of ocular surface reconstruction and assess the safety in cultivated oral mucosal epithelial cell sheet transplantation (COMET) regarding patients with cicatricial change of ocular surface.

NCT ID: NCT02126020 Withdrawn - Clinical trials for Stevens-Johnson Syndrome

Topical Infliximab in Autoimmune Eyes With Keratoprosthesis

Start date: November 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The Boston Keratoprosthesis type I (KPro) is a prosthetic cornea used to treat several causes of corneal blindness. Some categories of patients, including those with auto-immune diseases such as Stevens-Johnson syndrome, toxic epidermal necrolysis syndrome and mucous membrane pemphigoid, have a higher risk of failure for the KPro. Because of chronic inflammation, the cornea supporting the KPro may melt, leading to a higher risk of infection, loss of the KPro and loss of the eye. Infliximab is an antibody against tumor necrosis factor alpha and is used intravenously to control inflammation in several diseases. It has been used in some cases of corneal melting with significant success. This study's hypothesis is that infliximab can be successfully used as an eye drop (instead of the usual administration through veins) and that its regular use may prevent melt in eyes with a Boston Keratoprosthesis type I and underlying auto-immune disease.

NCT ID: NCT02037347 Terminated - Clinical trials for Stevens-Johnson Syndrome

Study to Evaluate the Use of Palifermin to Treat Toxic Epidermal Necrolysis

Start date: October 2010
Phase: Phase 1/Phase 2
Study type: Interventional

To test the ability of palifermin (a recombinant human keratinocyte growth factor) to decrease mucocutaneous injury and to promote epithelial repair in Toxic Epidermal Necrolysis and Stevens-Johnson Syndrome-Toxic Epidermal Necrolysis Overlap, diseases in which there is extensive sloughing of the skin and mucosa, including that of the eyes, gastrointestinal tract, respiratory and genitourinary systems.

NCT ID: NCT01696500 Completed - Clinical trials for Stevens-Johnson Syndrome

Phase III Clinical Trial of NPB-01 in Patients With Stevens-Johnson Syndrome/ Toxic Epidermal Necrolysis Unresponsive to Corticosteroids.

Start date: October 2012
Phase: Phase 3
Study type: Interventional

Patients diagnosed with Stevens-Johnson syndrome and Toxic Epidermal Necrolysis were confirmed based on the investigators national diagnostic criteria. Patients who meet all inclusion criteria and do not conflict with the exclusion criteria will receive NPB-01 (intravenous immunoglobulin) 400mg/kg/day for five consecutive days. Subsequently, efficacy of NPB-01 for therapy of Stevens-Johnson syndrome and Toxic Epidermal Necrolysis will be evaluated the disease evaluation score et al. As a safety endpoint, the safety of NPB-01 will be investigated the occurrence of adverse events by 20 days after the start of the study treatment.

NCT ID: NCT01582880 Completed - Clinical trials for Rheumatoid Arthritis

Use of Cross-linked Donor Corneas as Carriers for the Boston Keratoprosthesis

Start date: March 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the pilot study is to test the efficacy and safety of riboflavin/Ultraviolet A (UVA) cross-linked human donor corneas as carriers for the Boston Keratoprosthesis (Boston KPro) in patients with higher risk for corneal melting (keratolysis).

NCT ID: NCT01488396 Completed - Clinical trials for Stevens-Johnson Syndrome

Efficacy of 0.05% Cyclosporin Eye Drop in Stevens Johnson Syndrome Patient With Chronic Dry Eye

Start date: February 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy of 0.05% cyclosporin ophthalmic emulsion (Restasis) in patients with Stevens-Johnson syndrome that have dry eyes by subjective symptoms and signs.

NCT ID: NCT01256489 Withdrawn - Clinical trials for Stevens-Johnson Syndrome

Infliximab to Improve Retention of the Boston Keratoprosthesis in Patients After Stevens Johnson Syndrome/ Toxic Epidermal Necrolysis (SJS/TENS)

Start date: December 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The proposed study is intended to test the idea, based upon current knowledge of the biology and physiology of corneal ulceration in SJS/TENS patients who receive a keratoprosthesis, and on the known effects of infliximab on matrix metalloproteinases, that infliximab therapy for such patients may reduce the likelihood of corneal ulceration, and hence extend the period of prosthesis retention and vision recovery.

NCT ID: NCT01178242 Completed - Dry Eye Clinical Trials

Salivary Gland Transplantation in the Treatment of Dry Eye in Patients With Stevens-Johnson Syndrome.

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

The purpose of this study is to evaluate salivary gland and labial mucous membrane transplantation in patients with severe symblepharon and dry eye secondary to Stevens-Johnson Syndrome (SJS).

NCT ID: NCT01122303 Active, not recruiting - Clinical trials for Stevens-Johnson Syndrome

Corneal Epitheliotropic Factors in Autologous Serum Eye Drops in Nonautoimmune and Stevens-Johnson Syndrome With Dry Eye

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

Autologous serum eye drops (ASE) have been becoming popular in treatment of severe dry eye for the past decade. One of the most beneficial properties of the ASE over artificial eye drops is the epitheliotropic capacity owing to the presence of growth factors and other proteins. There have been reports on alteration of serum growth factors in autoimmune diseases such as rheumatoid arthritis. Alteration in serum growth factors may lead to different therapeutic effect of ASE. We therefore would like to know if there are any alteration growth factors, epidermal growth factor (EGF), transforming growth factor-beta1 (TGF-β1), transforming growth factor-beta2 (TGF-β2), and fibronectin, in ASE from Stevens-Johnson syndrome (SJS) patients with dry eye, which constitutes a major group of ASE usage in Siriraj Hospital, as compared with non-autoimmune dry eye. We also study stability of these factors following different storage conditions.