Phase
Condition
N/ATreatment
Silver I Alginate Non-Woven Dressing (Hydro-Alginate)
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Males or females, age 18 years or above. (Females must not be pregnant and if ofreproductive age should provide a negative pregnancy test at screening).
Patients who are able to understand and give informed consent to take part in thestudy.
Have one or more of the following: Pressure ulcer or Donor site wounds that areinfected, or are at high risk of infection (in the opinion of the Investigator),that are moderate to heavy levels of exudate.
Pressure ulcers that are moderate to high exudate, typically Category 3 and 4.
Only one primary wound may be treated per patient for the study.
Exclusion
Exclusion Criteria:
Patients who are known to be non-compliant with medical treatment,
Patients who are known to be sensitive to any of the device components
Subject is pregnant or actively breastfeeding;
Subject has a known sensitivity to Silver;
Life expectancy of <6 months;
Subject has any significant or unstable medical or psychiatric condition that, inthe opinion of the Investigator, would interfere with his/her ability to participatein the study;
Subject is currently enrolled in another clinical study, or has completed a clinicalstudy less than 30 days prior to enrolment.
Study Design
Study Description
Connect with a study center
Royal United Hospital Bath
Bath,
United KingdomSite Not Available
Royal United Hospital Bath
Bath 2656173,
United KingdomSite Not Available
Queen Victoria Hospital
East Grinstead,
United KingdomSite Not Available
Queen Victoria Hospital
East Grinstead 2650435,
United KingdomSite Not Available

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