Oasis Donor Site Wounds Post-Market Study

Recruiting N/A Interventional Study
Surgical Wound Wound Wounds and Injuries Wound Heal
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
16 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
40 (estimated)
Sponsor
Cook Biotech Incorporated · Industry
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About This Trial
The purpose of this study is to demonstrate the safety and performance of Oasis extracellular matrix (ECM) when used as a treatment for donor site wounds in the United Kingdom. Oasis ECM is commercially available for the treatment of partial and full-thickness skin wounds, including chronic wounds, wounds from trauma, and wounds that occur during surgery, such as donor site wounds. The ability of …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Has a split thickness skin graft (STSG) donor site wound no greater than 14 x 20 cm in size requiring placement of a covering material. 2. Has at least 24 hours to consent to study participation. Exclusion Criteria: 1. Age \< 16 years 2. Patients who, in the opinion of the …
Contacts

Carina Gregory, MS

765-497-3355

cgregory@rtix.com

CONTACT

Rae Ritchie, PhD

765-497-3355

rritchie@rtix.com

CONTACT