Ignite Creation Date:
2024-05-05 @ 11:48 AM
Last Modification Date:
2024-10-26 @ 9:13 AM
Study NCT ID:
NCT00137215
Status:
COMPLETED
Last Update Posted:
2008-07-28
First Post:
2005-08-25
Brief Title:
Evaluation of Silverlon Dressing for Autogenous Skin Donor Sites
Sponsor:
United States Army Institute of Surgical Research
Organization:
United States Army Institute of Surgical Research
Study Overview
Official Title:
Evaluation of Silverlon Dressing for Autogenous Skin Donor Sites
Status:
COMPLETED
Status Verified Date:
2008-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to compare one type of dressing against the current standard dressing that is used to cover an unburned area of the skin where a piece of skin is removed to cover another part of the body that was burned
Hypothesis The mean healing time for wounds treated with the Silverlon Dressing will be less than the mean healing time for wounds treated with Xeroform Dressing
Hypothesis The mean healing time for wounds treated with the Silverlon Dressing will be less than the mean healing time for wounds treated with Xeroform Dressing
Detailed Description:
At the time of the procedure donor sites that are symmetrical in size and shape will be selected Once the grafts have been harvested the wounds will be randomized for treatment using either the Silverlon dressing or Xeroform The wound dressings will then be observed at least once a day beginning 72 hours after surgery until healed defined as 90 or more of the wound surface being confluently re-epithelized
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None