Surgical Wound Clinical Trial
Official title:
Outcomes Comparing Different Methods of Skin Closure in Patients Undergoing Head and Neck Surgery.
Verified date | October 2017 |
Source | Boston Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
When patients undergo neck dissection surgeries, the current standard of care is to close the skin layer with either metal staples, which are removed a few days post-operatively, or with sutures, which can be absorbable or removed. To date, there is no conclusive data in the literature that definitively suggests one method is better than the other, with regard to wound complications or mature scar cosmesis. Currently, skin closure method is chosen by each individual surgeon, and is based on personal preference, factoring in evaluation of the wound. The goal of the study is to compare the two methods of skin closure, and the measured outcomes the investigators will be looking at are patient satisfaction, wound complications, and mature scar cosmesis. The investigators will be randomizing patients undergoing head and neck surgery to receive either staples or subcuticular sutures, and giving them surveys at their post-operative clinic visits to evaluate the outcomes, to determine if patients perceive one method to be superior to the other.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | March 2020 |
Est. primary completion date | March 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Able to provide informed consent - Ability to speak/read English language - Adult patients (age > 18) - Willing to have follow-up appointments (per clinical care protocol) - Both genders Exclusion Criteria: - Prior radiation therapy to the head and neck region (prior to surgery) - Prior surgery to the head and neck region (at the judgement of investigator) - Pregnancy |
Country | Name | City | State |
---|---|---|---|
United States | Boston Medical Center | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Boston Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Patient and Observer Scar Assessment Survey (POSAS) | Survey score - to assess for scar cosmesis outcome | 2 years post-operative | |
Secondary | Patient Satisfaction Survey | Survey score - to assess for patient satisfaction | 2 years post-operative | |
Secondary | Wound complications - dehiscence | Wound dehiscence | 2 years post-operative | |
Secondary | Wound complications - infection | Surgical site infections | 2 years post-operative |
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