Clinical Trials associated with Eosinophilic Fasciitis
NCT05915585
/ RecruitingNot ApplicableIIT
Efficacy of High-Intensity Laser Therapy for the Management of Eosinophilic Fasciitis: A Case Report
Eosinophilic fasciitis (EF) is a rare musculoskeletal disorder characterized by inflammation and thickening of the fascia, leading to pain, stiffness, and functional impairment. Conventional treatment options include immunosuppressive medications, corticosteroids, and physical therapy. This case report will describe use of high-intensity laser therapy (HILT) using the Mectronic Exand MY high-intensity laser system in a patient with EF, highlighting its potential as an alternative or adjunct treatment option.
The Influence of Extracorporeal Photopheresis on Skin Sclerosis - an Exploratory Clinical Study
Extracorporeal photopheresis (ECP), also known as extracorporeal photoimmunotherapy or photochemotherapy, is a leukapheresis-based therapy that has been in clinical use for over three decades after receiving FDA approval in 1988. Extracorporeal photopheresis was initially used for the treatment of T-cell lymphoma. Since its introduction, indications for initiating ECP were continuously extended to the treatment of Graft-versus-Host Disease (GvHD), systemic sclerosis, and in the field of solid organ transplantation. There is also evidence supporting the use of ECP in generalized morphea, a form of scleroderma limited to the skin, and in eosinophilic fasciitis, which is a rare, localized fibrosing disorder of the fascia. Concluding the results of the published studies, there is evidence that ECP has a positive effect on fibrosing disorders of the skin. Furthermore, in clinical practice, it has been observed that patients with systemic sclerosis, who undergo ECP treatment, show improvement of the skin lesions or a deceleration in the formation progress of such lesions during the therapy. Same findings can be observed in patients with sclerotic skin lesions of the skin, for example in the context of a GvHD. There are no clinical studies so far that describe these processes using objective measuring methods. Furthermore, the mechanism of action of ECP in systemic sclerosis and other fibrosing disorders with skin manifestations, has not yet been conclusively clarified. Serological markers for monitoring the progress of the therapy and determining the prognosis are also missing. Thus, a consensus regarding the frequency and duration of ECP for the therapy of systemic scleroderma or sclerotic diseases has not yet been reached. This study aims at evaluating the influence of Extracorporeal Photopheresis on the quality and functionality of sclerotic skin lesions assessed by several objective methods. Furthermore, potential biomarkers, which are being investigated in current studies, are to be determined in order to evaluate the influence of ECP on those biomarkers and better understand the mechanism of action of ECP on systemic sclerosis and fibrosing disorders involving the skin.
100 Clinical Results associated with Eosinophilic Fasciitis
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100 Translational Medicine associated with Eosinophilic Fasciitis
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0 Patents (Medical) associated with Eosinophilic Fasciitis
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Literatures (Medical) associated with Eosinophilic Fasciitis
01 Jan 2025·ACR Open Rheumatology
Clinical Images: Groove sign: heeding clue to eosinophilic fasciitis
Article
Author: Cui, Ran
01 Dec 2024·Skin Health and Disease
Clinical Signs and Utility of CT Pet Scan in Eosinophilic Fasciitis?
Article
Author: Adamson, Sarah R. ; Fong, Christopher ; Su, John C. ; Ng, Sally
A 61 year old male presented with clinical signs of Eosinophilic fasciitis (EF), a rare connective tissue disease. Early recognition of the diagnosis of EF is essential. Common examination findings are prayer sign and distal limb swelling, induration, venous guttering, and peau d'orange. CT PET scan can be helpful in supporting the diagnosis of EF.
01 Nov 2024·Actas Dermo-Sifiliográficas
[Translated article] Refractory Eosinophilic Fasciitis: Good Response to Ocrelizumab in a Patient with Multiple Sclerosis Under Treatment with Natalizumab
Article
Author: Hidalgo García, Y ; García Martínez, M ; Villafani Echazu, W J ; Vázquez Losada, B
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