Evaluate the Impact of Drawtex in Venous Leg Ulcers

Completed · Not applicable

Conditions studied: Moderatley to Highly Exuding Venous Leg Ulcers

In brief

This is a clinical study to comparatively evaluate the impact of Drawtex wound dressing against wound bioburden in moderately to highly exuding venous leg ulcers.

Key facts

Study ID

NCT01319123

Run by

Southwest Regional Wound Care Center

People needed

10

Starts

2010-10-01

Expected to finish

2011-08-01

Last updated by the study team

2012-10-30

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject > 18 years.
• Subject is attending weekly office visits at SW Wound Care Center as an out-patient.
• Subject has a moderately to highly exudative venous leg ulcer that would be indicated for treatment with Drawtex
• Subject or is informed about the trial, understands its nature of the study and provides written informed consent prior to study enrollment.
• Subject is willing and able to comply with all specified care and visit requirements

You may not qualify if…

• Subject has a lesion that does not meet the inclusion criteria.
• Subject refuses to participate in the study.
• Subject already participates in the this study with one wound (only one wound per subject is allowed)
• Subject has known sensitivity to the trial product or any of its compounds.
• Subject is expected to be non-compliant.
• Subject's lesion is a primary skin cancer.
• Subject's lesion is the manifestation of a metastasis.
• Subject is pregnant.

Where it is running

• Southwest Regional Wound Care Center — Lubbock, Texas, United States

Full record on ClinicalTrials.gov

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