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Scleroderma clinical trials

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NCT ID: NCT00319033 Completed - Clinical trials for Interstitial Lung Disease

Open-label Study With Bosentan in Interstitial Lung Disease

BUILD 2 OL
Start date: July 2004
Phase: Phase 2/Phase 3
Study type: Interventional

This study will asses the long term safety and efficacy of oral bosentan to patients suffering from Interstitial Lung Disease.

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: NCT00213525 Completed - Scleroderma Clinical Trials

Genesis of Scleroderma: Role of Environmental Factors in 100 Patients With Scleroderma and 300 Controls

Start date: October 2004
Phase: N/A
Study type: Observational

Scleroderma is an autoimmune disease of unknown origin. Recently, the role of environmental factors, and particularly toxic drug exposure, in the genesis of scleroderma has been suggested. This prompted us to conduct this prospective, case-control, multicentric study, including 2 groups of subjects: - 100 patients with scleroderma - 300 sex- and age-matched healthy controls. The aim of our study is to determine whether exposure to toxics is higher in patients with scleroderma compared with healthy controls.

NCT ID: NCT00204763 Terminated - Fecal Incontinence Clinical Trials

Comparison of Esophageal and Anorectal Manometry Catheters

Start date: January 2004
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to compare the accuracy of esophageal and anorectal manometric pressure measurements using a newly developed air filled balloon catheter with present standard solid state esophageal and anorectal catheters, respectively.

NCT ID: NCT00074568 Completed - Systemic Sclerosis Clinical Trials

Scleroderma Registry

Registry
Start date: September 2000
Phase:
Study type: Observational

Scleroderma is likely caused by a combination of factors, including an external trigger (infection or other exposure) and a genetic predisposition. The Scleroderma Registry will conduct genetic analyses for disease-related genes in patients with scleroderma and their family members (parents, brothers, and sisters).

NCT ID: NCT00043706 Completed - Systemic Sclerosis Clinical Trials

Safety, Tolerability, and Pharmacokinetics of CAT-192 (Human Anti-TGF-Beta1 Monoclonal Antibody) in Patients With Early Stage Diffuse Systemic Sclerosis

Start date: n/a
Phase: Phase 1/Phase 2
Study type: Interventional

Systemic Sclerosis (also known as Scleroderma) is a chronic, autoimmune disease of the connective tissue generally classified as one of the rheumatic diseases. Systemic Sclerosis causes fibrosis (scar tissue) to be formed in the skin and internal organs. The fibrosis eventually causes the involved skin to harden, limiting mobility, and can also damage other organs. Excess Transforming Growth Factor Beta-1 (TGF-beta1) activity may result in the abnormal fibrosis characteristic of Systemic Sclerosis. An antibody against TGF-beta1 may modify pathologic processes characterized by inappropriate fibrosis. Genzyme Corporation is currently investigating a human monoclonal antibody (CAT-192) that neutralizes active TGF-beta1. This study is being conducted in the U.S. and Europe to evaluate the safety, tolerability, and pharmacokinetics of repeated treatments with CAT-192 in patients with early stage diffuse Systemic Sclerosis.

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.

NCT ID: NCT00007267 Completed - Depression Clinical Trials

Psychological Treatments for Scleroderma

Start date: June 2001
Phase: Phase 2
Study type: Interventional

This study will examine the effectiveness of two psychological treatment approaches designed to help people who have scleroderma with three important areas of daily living: pain, depression, and distress about changes in appearance. The study will also evaluate the impact of depression on the two psychological treatments. Because psychological approaches requiring a trained professional can be expensive and are often not available to most patients, this study will also look at the effectiveness of a self-help treatment approach.

NCT ID: NCT00005675 Completed - Scleroderma Clinical Trials

Oral Type I Collagen for Relieving Scleroderma

Start date: April 2000
Phase: Phase 2
Study type: Interventional

Diffuse systemic sclerosis (SSc), or scleroderma, is a connective tissue disease causing damage to skin and other organs. The purpose of this study is to determine if taking oral bovine type I collagen (CI) will improve the condition of SSc patients.