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Stevens-Johnson Syndrome clinical trials

View clinical trials related to Stevens-Johnson Syndrome.

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NCT ID: NCT02795143 Withdrawn - Clinical trials for Toxic Epidermal Necrolysis

Evaluating the Effect of Isotretinoin in Regulatory T-cell Function in Adverse Cutaneous Drug Eruptions (ACDEs): A Pilot Study

Start date: November 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether isotretinoin is helpful in treating patients with an adverse cutaneous drug eruption known as toxic epidermal necrolysis (TEN).

NCT ID: NCT02319616 Withdrawn - Clinical trials for Toxic Epidermal Necrolysis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NCT ID: NCT02126020 Withdrawn - Clinical trials for Stevens-Johnson Syndrome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NCT ID: NCT01256489 Withdrawn - Clinical trials for Stevens-Johnson Syndrome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: NCT00372723 Withdrawn - Clinical trials for Toxic Epidermal Necrolysis

Study of a Potential New Treatment for Patients With Toxic Epidermal Necrolysis (TEN)

Start date: July 2006
Phase: Phase 2
Study type: Interventional

To determine whether treatment of patients who have toxic epidermal necrolysis with a drug called remicaide increases the number of patients who are alive 30 days laters.