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Fasciitis clinical trials

View clinical trials related to Fasciitis.

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NCT ID: NCT00441961 Completed - Fasciitis Clinical Trials

Treatment With High Dose Methotrexate in Patients With Eosinophilic Fasciitis

Start date: October 2006
Phase: N/A
Study type: Interventional

Evaluate the effect of high dose MTX on skin induration in patients with eosinophilic fascia.

NCT ID: NCT00382941 Completed - Tendinopathy Clinical Trials

Study of LED Phototherapy for Musculoligamentous Lesions

Start date: n/a
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether LED phototherapy using combined red and near infrared light (approved: Ministry of Health of Russian Federation No. 29/06070997/1080-00, EUROCAT Certificate No. CP033321-IV) is effective in the treatment of musculoligamentous lesions in physiotherapy practice

NCT ID: NCT00353275 Terminated - Clinical trials for Necrotizing Fasciitis

Hyperglycemia in Surgical Infections

Start date: August 2009
Phase: N/A
Study type: Interventional

The primary purpose of this study is to evaluate two glycemic control regimens on clinical outcome in patients with necrotizing soft tissue infections. Secondary aim is to evaluate the inflammatory and immune responses to the glycemic control regimens.

NCT ID: NCT00261807 Completed - Fournier's Gangrene Clinical Trials

Daptomycin for the Treatment of Severe Necrotizing Soft-Tissue Infections

Start date: June 2005
Phase: N/A
Study type: Interventional

Daptomycin is a new antimicrobial agent which has activity against resistant Gram positive cocci including MRSA. The phase 3 clinical trials for skin and soft tissue infections (SSTI) with Staphylococci and Streptococci have already demonstrated that daptomycin was noninferior to the comparator agent (vancomycin or beta-lactams) (10). Although this clinical trial did not include any patients with clostridial infection, there is in vitro data to support the activity of daptomycin against a variety of clostridial species(11) ( Clostridium perfringens) Therefore, for this trial we will include patients with clostridial infections with this species. Additionally, the patients in the SSTI study were not as ill as the proposed study population. Therefore for treatment of such severe infections, we would like to use a higher dose of daptomycin (6mg/kg/dose). The reasons for using a higher dose of daptomycin in this subgroup are as follows: 1. Patients who are severely ill have an increased volume of distribution; and therefore have a lower serum concentration of daptomycin. These patients might require a higher dose of daptomycin to achieve the desired serum concentration. 2. One of the organisms involved in necrotizing fasciitis is enterococcus (both-fecalis and faecium). E.faecium has higher MICs to daptomycin and would require a higher dose of the drug to achieve adequate free (unbound) serum concentration of the drug. 3. Both necrotizing fasciitis and endocarditis are serious deep seated infections. The clinical trials for endocarditis are using 6mg/kg/dose of daptomycin. Therefore for optimal treatment of necrotizing fasciitis, it is justifiable that we should use the higher dose of daptomycin. Objective: To evaluate the clinical and microbiological efficacy and safety of higher dose daptomycin therapy in the treatment of patients with severe necrotizing skin and soft tissue infections. Type of Study: Open label, single center study.

NCT ID: NCT00222911 Completed - Plantar Fasciitis Clinical Trials

Treatment of Plantar Fasciitis With Dorsiflexion Night Splints and Medial Arch Supports

Start date: August 2005
Phase: Phase 4
Study type: Interventional

The overall purpose of this study is to examine the combined effect of both dorsiflexion night splints and medial arch supports and compare it to the effect of these interventions each by itself in the treatment of plantar fasciitis.

NCT ID: NCT00189592 Completed - Plantar Fasciitis Clinical Trials

Plantar Fasciosis Treatment Using Coblation

Start date: August 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of Coblation-based fasciotomy for relieving pain associated with recurring plantar fasciosis and, secondarily, to determine whether there may be additional potential benefits stemming from its use.

NCT ID: NCT00155324 Completed - Plantar Fasciitis Clinical Trials

Change and Clinical Significance of Plantar Fascia Thickness After ESWT

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

The aim of the study is to investigate the effect of extracorporeal shock wave therapy (ESWT) on the thickness of plantar fascia measured by ultrasonographic examination among patients with chronic plantar fascitis. The change of plantar fascia thickness will be correlated with clinical improvement.