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Wegener Granulomatosis clinical trials

View clinical trials related to Wegener Granulomatosis.

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NCT ID: NCT00748644 Completed - Clinical trials for Microscopic Polyangiitis

Efficacy Study of Two Treatments in the Remission of Vasculitis

MAINRITSAN
Start date: October 2008
Phase: Phase 3
Study type: Interventional

Study of the efficacy of rituximab for maintenance treatment in systemic ANCA-associated vasculitis: prospective, multicenter, controlled, randomized comparative study of rituximab versus azathioprine

NCT ID: NCT00747461 Terminated - Sarcoidosis Clinical Trials

Interventional Cryotherapy for the Eradication of Benign Airway Disease ("ICE the BAD")

ICEtheBAD
Start date: October 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the safety, effectiveness, and side effects of the CryoSpray AblationTM System (CryoSpray AblationTM, "CSA" or "cryospray therapy") to treat benign airway disease in the lung using liquid nitrogen sprayed through a catheter via flexible fiber optic bronchoscopy (FFB)

NCT ID: NCT00647166 Completed - MPA Clinical Trials

Association Corticosteroid/Azathioprine in Microscopic Polyangiitis/ Polyarteritis Nodosa or Eosinophilic Granulomatosis With Polyangiitis (Churg Strauss Syndrome)

CHUSPAN2
Start date: May 2008
Phase: Phase 3
Study type: Interventional

To determine whether a combination of corticosteroids and azathioprine can achieve a higher remission rate and a lower subsequent relapse rate in patients with newly-diagnosed microscopic polyangiitis, polyarteritis nodosa or eosinophilic granulomatosis with polyangiitis (Churg Strauss syndrome) with no poor prognosis factor (FFS=0), and without significantly increasing the rate of adverse events, as compared to corticosteroids alone. The study hypothesis is a reduction of the absolute risk of treatment failure or relapse within the first 24 months following initiation of therapy of least 25%.

NCT ID: NCT00530075 Completed - Clinical trials for Wegener's Granulomatosis

Phase II Study on Gusperimus in Patients With Refractory Wegener's Granulomatosis

Start date: December 2003
Phase: Phase 2
Study type: Interventional

Wegener's granulomatosis is a primary systemic vasculitis characterized by granulomatous and necrotizing inflammation predominantly affecting the respiratory tract and the kidneys. Conventional therapy of Wegener's granulomatosis with cyclophosphamide and corticosteroids is limited by incomplete remissions and a high relapse rate. Patients accumulate irreversible damage due to the disease and the consequences of prolonged drug exposure. The efficacy and safety of an alternative immunosuppressive drug, gusperimus, was evaluated in patients with refractory disease. A prospective, international, nulti-centre, single limb, open label study. Entry required active Wegener's granulomatosis with a Birmingham Vasculitis Activity Score (BVAS) >=4 and previous therapy with cyclophosphamide or methotrexate. Immunosuppressive drugs were withdrawn at entry and prednisolone doses adjusted according to clinical status. Gusperimus, 0.5mg/kg/day, was self-administered by subcutaneous injection in six treatment cycles of 21 days with a seven day washout between cycles. Cycles were stopped early for white blood count < 4,000/mm3. The primary endpoint was complete remission (BVAS=0 for at least 2 months) or partial remission (BVAS<50% of entry score). After the sixth cycle azathioprine was commenced and follow-up continued for a further six months.

NCT ID: NCT00468208 Completed - Clinical trials for Wegener's Granulomatosis

Abatacept in Treating Adults With Mild Relapsing Wegener's Granulomatosis

Start date: February 2008
Phase: Phase 1/Phase 2
Study type: Interventional

Wegener's granulomatosis (WG) is a rare disease that causes inflammation of blood vessels, or vasculitis. It may involve many different parts of the body, but typically affects the upper and lower respiratory tract and kidneys. The purpose of this study is to determine the safety and effectiveness of the medication abatacept in treating adults with mild relapsing WG.

NCT ID: NCT00430105 Completed - Clinical trials for Microscopic Polyangiitis

Pulse Versus Continuous Cyclophosphamide for Induction of Remission in ANCA-Associated Vasculitides

Start date: February 1998
Phase: Phase 2/Phase 3
Study type: Interventional

A comparison of intermittent pulsed cyclophosphamide to daily oral cyclophosphamide for the treatment of ANCA-associated systemic vasculitides with kidney involvement. Performed by the European Vasculitis Study group.

NCT ID: NCT00349674 Active, not recruiting - Clinical trials for Systemic Wegener's Granulomatosis

WEGENT - Comparison of Methotrexate or Azathioprine as Maintenance Therapy for ANCA-Associated Vasculitides

Start date: January 1999
Phase: Phase 3
Study type: Interventional

Remission of ANCA-associated vasculitis can be obtained in approximately 80% of the patients with a combination of corticosteroids and cyclophosphamide. However, relapses are frequent. This point warrants the prescription of a maintenance treatment with a less toxic immunosuppressant for several months to years. The optimal drug in this indication is not determine. We decided therefore to compare the 2 most used drugs in this indication. Induction therapy consists in the combination of corticosteroids and intravenous cyclophosphamide pulses. Corticotherapy consisted first in one daily methylprednisolone pulse, for 1 to 3 days, followed by oral prednisolone at the dose of 1 mg/kg/d for 3 weeks, then progressively tapered and stopped at the 18th month from the diagnosis. Cyclophosphamide is administered every 2 weeks for the first 3 bolus (0.6 g/m2 - D1, 15 and 30), then every 3 weeks (0.7 g/m2). Once remission is achieved, patients receive 3 additional bolus (0.7 g/m2). At that time, patients are randomized for a maintenance treatment with azathioprine (2 mg/kg/d, orally) or oral methotrexate (starting at the dose of 0.3 mg/kg/wk, then progressively increased every weeks by 2.5mg, if necessary, to a maximum and optimal dose of 25 mg/wk) for 12 months.

NCT ID: NCT00307671 Completed - Vasculitis Clinical Trials

Treatment of Necrotizing Vasculitides for Patients Older Than 65 Years

CORTAGE
Start date: July 2005
Phase: Phase 4
Study type: Interventional

The aim of this trial is to lower the morbidity rate in elderly patients affected with systemic necrotizing vasculitides, by reducing mortality and improving global outcome.

NCT ID: NCT00307593 Completed - Clinical trials for Microscopic Polyangiitis

RATTRAP: Infliximab Versus Rituximab in Systemic Necrotizing Vasculitides

Start date: May 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to compare a 2 immunosuppressant regimen for the treatment of relapsing or refractory necrotizing antineutrophil cytoplasmic antibody (ANCA) associated vasculitides.

NCT ID: NCT00138983 Completed - Clinical trials for Rheumatoid Arthritis

Prevention of Glucocorticoid-Induced Osteoporosis in Rheumatic Diseases: Alendronate Versus Alfacalcidol.

Start date: May 2000
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine wich treatment is the most effective in prevention of glucocorticoid-induced osteoporosis in patients with rheumatic diseases. The STOP-study: a randomized placebo controlled trial with alendronate versus alfacalcidol.