Clinical Trials Directory

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UnknownNCT00938691

Optimal Suture Choice for Improved Scar Outcomes

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
25 (actual)
Sponsor
Dallas VA Medical Center · Federal
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Certain parts of the body, such as the chest, back, and shoulders, are notorious for producing cosmetically poor scars after cutaneous surgery. While very little research has been done to understand these poor outcomes, it is generally thought that increased tension across the skin inherent to these body areas leads to significant widening of the final scar. Historically, the only way to combat this tension was to support the deeper portion of the wound with sutures that dissolve over several weeks. However, scars take many months to fully develop their greatest strength. So even with the standard technique, wounds in areas of high tension still show spreading of the scar with time. The investigators believe that these wounds require an extended duration of support throughout the scar's maturation period. Until recently, there did not exist a suture that could provide this long duration of support without also carrying the risk of the body rejecting it. Recently, a new extremely long acting absorbable biomaterial has been FDA approved for use as a suture. The investigators plan to use this suture to test the theory that alleviating stress on high tension wounds throughout the period which they gain their maximal integrity produces less scar spread and ultimately better cosmetic outcomes.

Conditions

Interventions

TypeNameDescription
PROCEDUREIntradermal Suture
PROCEDUREIntradermal Suture

Timeline

Start date
2009-04-01
Primary completion
2010-06-01
Completion
2010-07-01
First posted
2009-07-14
Last updated
2009-07-14

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00938691. Inclusion in this directory is not an endorsement.