This is a 24-week observational follow safety study for Study 802-247-09-015.
The objective of this study is to examine the durability of previous target wound closures, identify new test article-related adverse events, record new target wound closures, and examine ongoing adverse events not resolved in subjects who participated in HP 802-247-09-015.
Study Type
OBSERVATIONAL
Enrollment
206
The Number of Participants With Closed Target Ulcers at Each Visit
At each visit the status of closed target ulcers was evaluated as remained closed or re-opened.
Time frame: Over the 24-week study period, at each of the bi-monthly visits
Number of Subjects With Target Wound Closed for the First Time During the Study Period.
At each visit the status of open target ulcers was evaluated as "remained open" or "closed".
Time frame: Over the 24-week study period, at each of the bi-monthly visits
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University of AZ College of Medicine
Tucson, Arizona, United States
Center for Clinical Research
Castro Valley, California, United States
ILD Consulting, Inc.
Encinitas, California, United States
Vascular Surgery Associates
Los Angeles, California, United States
UCSD Wound Treatment and Research Center
San Diego, California, United States
University of Miami
Miami, Florida, United States
Doctors Research Network
South Miami, Florida, United States
Robert J. Snyder
Tamarac, Florida, United States
Northwestern University Feinberg School of Medicine
Chicago, Illinois, United States
Passavant Area Hospital
Jacksonville, Illinois, United States
...and 20 more locations