Restore Calcium Alginate Dressing, Silver vs Aquacel Ag in the Treatment of Critically Colonized Venous Leg Ulcers
Status: | Completed |
---|---|
Conditions: | Other Indications, Cardiology, Infectious Disease, Gastrointestinal |
Therapuetic Areas: | Cardiology / Vascular Diseases, Gastroenterology, Immunology / Infectious Diseases, Other |
Healthy: | No |
Age Range: | Any |
Updated: | 2/4/2013 |
Start Date: | October 2011 |
End Date: | March 2013 |
Contact: | Mary B Regan, PhD |
Email: | mary.regan@hollisterwoundcare.com |
Phone: | 727 385 2904 |
Calcium alginate dressings with silver have been found to be safe and effective for use for
leg ulcers. The primary objective is to compare Restore Calcium Alginate Dressing, Silver to
AqualCel Ag Dressing on the following parameters: No further progression toward infection
(bioburden), ease of application and removal, and percent progression to closure. The
secondary objective is to obtain photographic documentation of the leg ulcers during the
course of the study.
Inclusion Criteria:
1. Is 18 years or older; male or female.
2. Previous diagnosis of venous insufficiency proven by a positive venous duplex with
reflux.
3. Has a venous ulcer with a wound area between 5 cm2 - 40 cm2.
4. Has an ankle brachial index (ABI) >0.8.
5. Has a venous ulcer with duration less than 24 months.
6. Has a venous ulcer which is critically colonized (not infected) based on the Lazareth
Study Model. Ulcers are considered to be critically colonized if at least three of
the five following signs are present:
Severe spontaneous pain between two dressing changes,Perilesional erythema,Local
edema,Malodour,Heavy Exudation
7. Is currently using Profore as their standard of care.
8. Has not received antibiotics for 6 weeks prior to enrollment.
Exclusion Criteria
1. Has an allergy to one of the components of the dressings (calcium alginate,
hydrocolloid [carboxymethylceullose], silver).
2. Is currently on antibiotics.
3. Has a negative venous duplex.
4. Is unable to tolerate 4 layer compression.
5. Is unable to continue contact with the investigator for a period of at least two
weeks.
6. Is unwilling or unable to comply with the study protocol.
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