Mohs Surgery Clinical Trial
Official title:
Use of a Novel Device for Stretch Relaxation During Mohs Surgery
Closure of cutaneous defects is associated with many common and serious problems. For
example, Mohs surgery involves the removal of skin and other soft tissues that have been
proven to be infiltrated with cancer. Iterative stages of Mohs are processed and examined
microscopically for residual tumor. Using specialized mapping, the surgeon can effectively
achieve a high cure rate and minimize removal of unaffected tissue. This process usually
takes a total of 2-3 hours, since the patient waits while the tissue is being processed, and
complete clearance of margins can take multiple stages. In many cases, a cutaneous defect is
produced of significant size. In certain areas of high tension, such as scalp and lower leg,
this mandates either a lengthy course of wound care or that the surgeon perform a graft or
flap. In many cases, performance of a graft is undesirable due to lack of vascularity to
support graft survival. Creation of flaps involves incision and undermining of large areas of
tissue in order to achieve wound closure. There is a current need for alternatives to graft
and flaps in these locations.
Human skin has biomechanical properties that can be harnessed to facilitate closure of larger
wounds. Stress-relaxation refers to the natural relaxation exhibited by skin put under a
given amount of tension (stress) over time. After a period of stress, the force required to
close the wound is reduced. In a porcine skin wound model, there is a 40-60% reduction in
stress after twenty minutes of stretch relaxation.
There are several classic methods of delivering this stretch to skin intraoperatively. Most
simply, a towel clamp can be used to bring edges together. However, the clamp, which is a
sharp stainless steel instrument, can damage tissues. There are also commercial devices such
as TopClosure. However, this device is intended for very large wounds with side plates that
must be sutured or stapled to patient skin.
The SUTUREGARD device presents a simple method to provide stress to a wound but not damage
tissue. The SUTUREGARD device results in significantly lower pressure on the skin when
compared with traditional sutures and creates a much greater volume of wound eversion than is
possible with a traditional suturing method. Engineering tests performed at OSU showed that a
given simple interrupted suture will exert about 30% less pressure on the skin when used
performed with the device compared to without the device. With this protection, this creates
the corollary that a suture could be safely tied to a greater force with the device than
without. In animal testing, the device has been used on porcine wounds for up to 6 weeks,
where it showed superior histologic tolerability over traditional sutures.
The investigators have used the device to provide stress-relaxation within our clinic over
the past several months and have seen reductions in wound width of about 30% with retention
of the device for 30-60 minutes. Wounds exhibit significantly more reduction in width with
overnight use. Unlike traditional retention sutures, which damage the skin, the skin appears
normal with retention of the device for up to 2 days in our patients. Furthermore, all wounds
that have been stress-relaxed with the device have healed without complication.
The investigators plan to study the stress-relaxation created by use of a SUTUREGARD device
applied to cutaneous defects for a specified time periods (30, 60 and 90 minutes).
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