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Leg Ulcer clinical trials

View clinical trials related to Leg Ulcer.

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NCT ID: NCT02896725 Completed - Varicose Ulcer Clinical Trials

Wool-derived Keratin Dressings for Venous Leg Ulcers

Keratin4VLU
Start date: March 1, 2017
Phase: N/A
Study type: Interventional

Venous leg ulcers (VLU) are the most common leg ulcer, can be painful, and limit work, lifestyles and activity, especially in older patients. Compression bandaging is the main treatment but there are few added treatments for patients with slow healing VLU. About 50% of patients with VLU may be slow healing. Research suggests using keratin dressings as well as using compression may help healing in patients with show healing VLU, but the current evidence is not enough to change clinical practice. The investigators will conduct a randomised controlled trial to test whether using keratin dressings is better than usual care for slow healing VLU.

NCT ID: NCT02889926 Active, not recruiting - Leg Ulcer Clinical Trials

Utility of Samples in Bacteriological Prospective Series of Ulcers Leg Infected Clinically

ULCERINFECTE
Start date: February 10, 2017
Phase: N/A
Study type: Interventional

Leg ulcers are defined as wounds lasting for more than a month. They would receive 0.2% of the population of Western countries. In Europe, the cost per episode of leg ulcers is estimated at 6650 euros (10 000 euros for a foot ulcer). The cost of treatment of wounds would be 2 to 4% of the health budget. Infection is the most common complication of chronic wounds: in most cases, it results in delayed healing, at most, it can result in amputation or serious general complications Bacterial contamination of ulcers is constant. Over time for over 25 years, various studies have shown about relatively identical results. The bacteria are present in over 90% of the etiology of venous leg ulcers. These bacteria are divided into four most common classes: Staphylococcus aureus, Enterococcus, Streptococcus, Pseudomonas. The bacterial ecology changes over time. Indeed Staphylococcus aureus appears first, while the Pseudomonas is associated with ulcers lasting for several months. Anaerobic more difficult to find, are found in 30% of cases Cohabitation between leg ulcers and bacteria often without clinical consequence: These are the stages of infection and colonization. The infection is related to the proliferation of bacteria and their invasion into the skin, by increasing their virulence (virulence genes acquisition). The increase in the number of bacteria and the multiplicity of bacterial genera are one reason for the increased virulence of bacteria. When bacteria proliferate, because the host defenses are inadequate, or because there is a vascular disease which promotes the proliferation, clinical signs appear

NCT ID: NCT02884323 Completed - Venous Leg Ulcer Clinical Trials

A Study in Patients With Venous Leg Ulcers and Measuring the Effects of Using Geko™ Device

Start date: August 2016
Phase: N/A
Study type: Interventional

This is a single centre open label study measuring lower limb physiology in patients with venous leg ulcers at the University Hospital of South Manchester. Ambulatory venous pressure, venous transit times, wound bed tissue oxygenation and changes in microcirculation will be measured at baseline after the gekoTM device is activated. Ambulatory venous pressure and venous transit times will be performed whilst the participant is standing, sitting and supine

NCT ID: NCT02873728 Not yet recruiting - Leg Ulcer Clinical Trials

Remote Ischemic Conditioning for Treatment of Chronic Wounds

Start date: November 2016
Phase: N/A
Study type: Interventional

The goals of this series of studies is to test the effect of RIC on chronic leg ulcers (Diabetic ulcers and venous ulcers) - and to improve the understanding of its biological mechanism. This is a prospective, double-blind, randomized, shame procedure-controlled study.

NCT ID: NCT02863068 Completed - Sickle Cell Disease Clinical Trials

Topical Sodium Nitrite in Sickle Cell Disease and Leg Ulcers

Start date: April 6, 2018
Phase: Phase 2
Study type: Interventional

The investigators are conducting a Phase II prospective and placebo controlled study of a topical cream containing sodium nitrite compared to the current standard of care. Sodium nitrite is a local donor of nitric oxide, which is known to improve blood flow and decrease bacterial load in the ulcer bed. The primary objectives are to evaluate the safety of topical sodium nitrite cream treatment in patients with sickle cell disease and chronic leg ulcers and to determine its effectiveness in accelerating the healing process and decreasing the pain associated with ulceration. Potential benefit will be a durable resolution or improvement of the leg ulcer and its associated pain. Possible side effects include decreased blood pressure and methemoglobinemia, secondary to sodium nitrite absorption through the ulcerated skin. Funding source FDA OOPD.

NCT ID: NCT02842502 Recruiting - Leg Ulcer Clinical Trials

Clinical Feasibility of an Advanced Therapy Medicinal Product (ATMP) Preparation for Autologous Skin Regeneration in Case of Chronic Leg Ulcers

MecaSkin
Start date: September 2014
Phase: N/A
Study type: Interventional

This study deals with the feasibility of an ATMP (Advanced Therapy Medicinal Product) production for the treatment of chronic wounds ulcer. Recruitment concerns patients (n=7) with leg ulcers and receiving a skin pellet graft. During surgical procedure, supernumerary biopsies are planned to be done in order to be transferred to laboratory. Then, the possibility of cell extraction (keratinocytes and fibroblasts), expansion, banking and use for skin substitute production in clinical condition is evaluated (primary outcome).

NCT ID: NCT02813187 Enrolling by invitation - Venous Stasis Ulcer Clinical Trials

Venous Leg Ulcer and Lymphedema Registry

VLULR
Start date: May 2016
Phase:
Study type: Observational [Patient Registry]

This is an observational, longitudinal real world registry of venous leg ulcers created from electronic health record data obtained in the course of clinical care. Data from certified electronic health records transmit data as part of the requirement to share data with a specialty registry under Objective 10 of Meaningful Use of an EHR.

NCT ID: NCT02798445 Not yet recruiting - Venous Ulcer Clinical Trials

TAPIRS Technique Plus Adjustable Compression System in Treatment of Venous Leg Ulcers

TAPIRS
Start date: June 2016
Phase: N/A
Study type: Interventional

The aim of this study is to determine the percentage of healing of active venous ulcers following Terminal Axial Perforator Interruption Reflux Source (tapirs technique) and adjustable compression system versus a control group using the traditional multilayer bandages.

NCT ID: NCT02782689 Terminated - Venous Leg Ulcer Clinical Trials

Clinical Study to Assess Efficacy and Safety of a New Compression System in the Management of Venous Leg Ulcers

COMPULCE
Start date: June 2014
Phase: N/A
Study type: Interventional

The primary objective of this study is to demonstrate the non-inferiority of the 2-layer compression system Kit Biflex® with regard of the 4-layer compression system PROFORE® in the treatment of venous leg ulcers in terms of complete healing at 16 weeks.

NCT ID: NCT02729688 Completed - Clinical trials for Venous Insufficiency

Effectiveness of a Pressure Indicator Guided and a Conventional Bandaging in Treatment of Venous Leg Ulcer

Start date: March 2016
Phase: N/A
Study type: Interventional

Objective of this study are to compare the interface pressure by applying ordinary elastic bandage (OEB) and CPG-EB. In addition, investigators compared the percentage of patients who could apply the optimal pressure with OEB and CPG-EB.