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The purpose of this study is to test wounds found on the outside of the body surface with an investigational medical imaging device that collects visual pictures and thermal digital pictures of the wound site. The investigational device has not been approved by the Food and Drug Administration (FDA).
The medical imaging device is non-contacting and is non-radiating (delivers no energy to the body). It passively collects pictures (typical digital color photographs)and thermal pictures (black and white digital photographs of heat at the body surface.)
Full description
This prospective study utilizes the WoundVision Wound Measuring and Monitoring System (WMMS) to study external wounds, which can currently be measured for length by width using a ruler. WMMS operates by taking simultaneous visual and thermal images of the external wound site and the associated body surface. These images are evaluated by utilizing the WMMS ImageReview measuring and monitoring software. WMMS ImageReview software allows for LxW (length by width) and surface area (cm squared),as well as perimeter (cm) external wound measurements of the visual image. WMMS ImageReview software also allows for the display of thermal intensity variation data for the associated body surface of the corresponding thermal image.
This study is primarily designed to utilize the Coefficients of Individual Agreement (CIA)as a means of establishing the equivalence of area measurements utilizing the WMMS ImageReview software LxW technique and the current "gold standard" LxW manual ruler technique.
A secondary objective measures the thermal intensity variation data of the external wound bed by overlaying the corresponding "Visual External Wound Trace"from the visual image onto the thermal wound bed.
Enrollment
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Inclusion criteria
Age 18 or greater, of either gender and of any ethnic background
Able to tolerate position changes and turns for up to 10 minutes comfortably
Have an existing external wound that is currently measured for length and width using a ruler
Have qualifying external wound sites:
Exclusion criteria
Neonatal and pediatric patients
Pregnant women
Cannot tolerate position changes for up to 10 minutes comfortably (per external wound site imaged)
Cannot be positioned so images can be taken at approximately 90 degrees perpendicular and 18 inches away from the external wound site
On therapies or treatments which cannot be safely suspended long enough to conduct an imaging session as determined by facility policy
Have external wound dressing or medical device which cannot or should not be removed as determined by site investigator
Have an external wound with excessive or heavy exudate that cannot be controlled during the imaging session. Excessive drainage can obscure external wound features
Have complex external wound site(s):
Have not provided signed informed consent
Non-English speaking
Primary purpose
Allocation
Interventional model
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40 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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