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Varicose Ulcer clinical trials

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NCT ID: NCT01376050 Terminated - Venous Stasis Ulcer Clinical Trials

Efficacy Study of the Application of Low Level Laser Light to Treat Venous Stasis Ulcers

Start date: June 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether low level laser light therapy is effective as an adjunctive therapy to the healing of venous stasis leg ulcers.

NCT ID: NCT00998673 Terminated - Venous Ulcer Clinical Trials

Silica Gel Fiber Wound Dressing for Chronic Venous Leg Ulcers

Start date: April 2009
Phase: Phase 2
Study type: Interventional

Silica Gel Fiber is a bioresorbable, inorganic silica gel fibre patch promoting skin tissue growth and enhanced wound healing for all types of chronic wounds. It is applied as patch and will be hold in place by a secondary dressing for maintaining the moist wound environment. The study is aimed to demonstrate superiority over a standard wound treatment for chronic venous leg ulcers. The primary efficacy variable is time to healing.

NCT ID: NCT00847002 Terminated - Venous Ulcer Clinical Trials

Flexitouch Treatment for Venous Ulcers

Start date: September 2007
Phase: N/A
Study type: Interventional

This is a study to compare the healing process of venous stasis ulcers when the Flexitouch® system is added to the standard treatment of venous ulcers. We hypothesize that adding the Flexitouch® system to standard venous ulcer treatment will result in 1. greater complete healing 2. greater percentage reduction in ulcer area 3. reduced time to complete healing, as compared to the use of standard treatment alone 4. a greater reduction in affected leg volume as compared to standard treatment alone.

NCT ID: NCT00727701 Terminated - Varicose Ulcer Clinical Trials

Study of Individualized Wound Prevention Instruction to Prevent Venous Ulcer Development

Start date: July 2008
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether individualized wound prevention instructions will lengthen the ulcer-free period in veterans with recently healed venous ulcers.

NCT ID: NCT00613808 Terminated - Venous Ulcers Clinical Trials

Safety and Efficacy of Gaseous Nitric Oxide on Venous Stasis Leg Ulcers

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

The purpose of this study is to determine whether nitric oxide (NO)gas is effective in the treatment of venous ulcers of the lower leg.

NCT ID: NCT00545298 Terminated - Venous Ulcers Clinical Trials

Safety and Efficacy of Gaseous Nitric Oxide on Venous Stasis Leg Ulcers

Start date: October 2007
Phase: Phase 2
Study type: Interventional

This study will test the safety and efficacy of nitric oxide gas in the treatment of venous leg ulcers

NCT ID: NCT00534937 Terminated - Venous Stasis Ulcer Clinical Trials

Flexitouch Compression System for Venous Stasis Ulcer

Start date: September 2007
Phase: Phase 4
Study type: Interventional

The researchers hypothesize that utilization of the Flexitouch system will improve the healing rates of (venous stasis ulcers) VSU compared to traditional compression wrapping therapy alone. Primary Objective: The primary study objective is to determine whether the complete healing rate of venous stasis ulcers at 12 weeks is improved by the addition of Flexitouch® System compression therapy to a standard regimen of compression wrapping. Secondary Objectives: - To determine whether the addition of Flexitouch System compression therapy to a standard regimen of compression wrapping increases the percentage reduction in wound surface area. - To determine whether the addition of Flexitouch compression therapy to a standard regimen of compression wrapping increases the percentage reduction in volume of the affected limb. - To determine whether the addition of Flexitouch compression therapy to a standard regimen of compression wrapping decreases the time to healing of the venous stasis ulcer.