Evaluation of Exufiber Ag + and Other Gelling Fibre Dressing



Status:Recruiting
Conditions:Hospital
Therapuetic Areas:Other
Healthy:No
Age Range:18 - Any
Updated:3/9/2019
Start Date:August 14, 2017
End Date:December 30, 2019
Contact:Tina Kjellen
Email:tina.kjellen@molnlycke.com
Phone:+46317223000

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A Clinical Investigation to Study the Effect of Exufiber Ag+ and Other Gelling Fibre Dressings on Wound Exudate in Medium to High Exuding Wound

Investigate impact of gelling fiber dressings on handling exudate in medium to high exuding
wounds


Inclusion Criteria:

- Signed Informed Consent Form

- Both gender ≥ 18 years old

- From Medium to High exuding wound

Exclusion Criteria:

- Known allergy or hypersensitivity to any of the treatment dressings

- Pregnant or lactating females

- Subjects with a target wound that is ≤1 cm2

- Subjects with a target wound that is a full thickness burn

- Subjects with a target wound that is a full thickness pressure ulcer

- Subjects with known immunodeficiency

- Subject taking systemic antibiotics for wound infection

- Subject were the target wound is located on an infected limb interfered by minimal
blood flow in the opinion of the investigator

- Subject with a target wound with unexplored enteric fistula

- Subjects who in the opinion of the investigator, will have problems following the
protocol

- Subjects needing treatment with oxidizing agents such as hypochlorite solutions or
hydrogen peroxide

- Previously enrolled in the present investigation

- Inclusion in other ongoing investigations at present that would preclude the subject
from participating in this investigation as judged by the investigator

- Involvement in the planning and conduct of the clinical investigation
We found this trial at
1
site
San Francisco, California 94115
Principal Investigator: Alexander Reyzelman
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mi
from
San Francisco, CA
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