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Scleroderma, Diffuse clinical trials

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NCT ID: NCT00282425 Terminated - Scleroderma Clinical Trials

Allogeneic Hematopoietic Stem Cell Transplantation (NST) for Patients With Systemic Sclerosis

Start date: May 2005
Phase: Phase 1
Study type: Interventional

Scleroderma is disease believed to be due to immune cells, cells which normally protect the body but are now causing damage to the body. There has not been any treatment that has been effective in treating this disease. The likelihood of progression of the disease to severe disability and death is high. This study is designed to examine whether treating patients with high dose Cyclophosphamide and Fludarabine (drugs which reduce the function of your immune system) and CAMPATH-1H (a protein that kills the immune cells that are thought to be causing the disease), followed by return of blood stem cells that have been previously collected from patients brother or sister will stop or reverse the disease. The purpose of the Cyclophosphamide, Fludarabine and CAMPATH-1H is to decrease immune system. The purpose of the stem cell infusion is to restore blood production, which will be severely impaired by the Cyclophosphamide, Fludarabine and CAMPATH-1H, and to produce a normal immune system that will no longer attack the body.

NCT ID: NCT00226889 Terminated - Clinical trials for Systemic Sclerosis (Scleroderma)

Treatment of Early Systemic Sclerosis by Bosentan

TRANOS
Start date: January 2005
Phase: Phase 1/Phase 2
Study type: Interventional

Systemic sclerosis (ssc) is characterised by extensive tissue fibrosis. Using drugs that are capable of inhibiting fibroblast activity may be beneficial if administrered early in the disease course. Thirty adult patients with early SSc will be treated with the endothelin-1 antagonist bosentan for 6 months.Disease progression will be assessed.

NCT ID: NCT00040651 Terminated - Systemic Sclerosis Clinical Trials

Safety and Value of Self Bone Marrow Transplants Following Chemotherapy in Scleroderma Patients

Start date: July 2002
Phase: Phase 1
Study type: Interventional

Scleroderma, or systemic sclerosis (SSc), is a diffuse connective tissue disease characterized by changes in the skin, blood vessels, skeletal muscles, and internal organs. The purpose of this study is to determine the safety and value of self bone marrow transplants after chemotherapy in patients with severe SSc.