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Leg Ulcers clinical trials

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NCT ID: NCT00628004 Completed - Leg Ulcers Clinical Trials

Safety Evaluation of Biatain Ibu in Painful Chronic Venous Leg Ulcers

Start date: May 2008
Phase: N/A
Study type: Interventional

The objective of this open label extension study (extension to study DK143WS) is to evaluate the safety of Biatain Ibu during 6 -12 weeks of exposure and during a 40 - 46 weeks safety follow-up period.

NCT ID: NCT00522002 Completed - Clinical trials for Rheumatoid Arthritis

CLUE Study: Connective Tissue Disease Leg Ulcer Etiology Study

CLUE
Start date: August 2007
Phase: N/A
Study type: Observational

To explore the hypothesis that leg ulcers are associated with hypercoagulable states, the CLUE study will evaluate patients with connective tissue disease associated leg ulcers, to identify risk factors (especially hypercoagulability and immunologic characteristics), characterize pathogenesis, predict response to therapy, and assess the impact of lower extremity ulcers on quality of life.

NCT ID: NCT00184873 Completed - Leg Ulcers Clinical Trials

Legtest Multi Centre Testing of the Lively Legs Program for Promoting Compliance in Leg Ulcer Patients

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

Leg ulcers are often chronic or recurring complications of peripheral circulation disorders. Patients' lifestyles are known to influence leg ulcer occurrence and circulation disorders in general. Especially exercise and compliance with compression therapy are key elements in the course of leg ulcer healing and recurrence. Yet many patients demonstrate sedentary lifestyles and non-compliance and current practice offers no systematic approach in the promotion of compliance and physical activity in these patients. The purpose of the study is testing 'Lively Legs' a compliance promotion program for patients with leg ulcers. The study tests the program on effects regarding: - compliance with compression therapy and exercise levels - time to leg ulcer recurrence - cost effectiveness from a social perspective.

NCT ID: NCT00007280 Completed - Leg Ulcers Clinical Trials

Bioengineered Skin and Wound Healing

Start date: October 2000
Phase: Phase 1
Study type: Interventional

This study will look at whether a graft of bioengineered skin (BSC), known commercially as Apligraf, stimulates the healing process in a person's own skin at the edge of a wound (known as the edge effect). The information from this study will provide a better understanding of the ways that grafts of bioengineered skin help the healing of chronic wounds. We will assign study participants to either the bioengineered skin group or the control group. People in the control group will receive compression therapy with a multilayered compression bandage. We will examine each participant before starting treatment and then once a week for 24 weeks or until the wound heals. On the first day of treatment (day 0) and at week 3, week 6, and week 24 (end of treatment) we will take a small tissue sample from the wound for a biopsy. After the wound is completely healed, we will ask the patient to return once a month for 6 months to make sure the wound stays healed.