Orthopaedic Surgical Wound Closure Comparison Study
Primary Purpose
Incision, Surgical
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Suture
Clozex
Zipline
Sponsored by
About this trial
This is an interventional treatment trial for Incision, Surgical
Eligibility Criteria
Inclusion Criteria:
- Age 18+
- Patient scheduled to undergo elective orthopaedic surgical procedure with a minimum anticipated incision length of 3 cm.
- Willingness and ability to comply with scheduled visits and study procedures.
Exclusion Criteria:
- Revision Surgery
- Compromised wound healing (autoimmune disorder, chronic steroids, connective tissue disorder)
- Pregnant women, fetuses, neonates, children, prisoners, cognitively impaired, educational or economically disadvantage, non-English speaking subjects.
Sites / Locations
- University of Virginia
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
Suture
Adhesive wound closure device
Adhesive wound closure device with zip ties
Arm Description
Standard suture wound closure
Clozex wound closure device
Zipline wound closure device
Outcomes
Primary Outcome Measures
Stony Brook Scar Evaluation Scale
Scores range from 0-5. Higher scores indicate better scar healing. Lower scores indicate worse scar healing
Secondary Outcome Measures
Full Information
NCT ID
NCT05251064
First Posted
January 21, 2022
Last Updated
February 17, 2022
Sponsor
University of Virginia
1. Study Identification
Unique Protocol Identification Number
NCT05251064
Brief Title
Orthopaedic Surgical Wound Closure Comparison Study
Official Title
Randomized Controlled Trial of Wound Closure Techniques in Orthopaedic Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
April 23, 2019 (Actual)
Primary Completion Date
January 20, 2022 (Actual)
Study Completion Date
January 20, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Virginia
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study is trying to find out if there is one method of surgical incision closure is better than another. The three different wound closure methods in this study are currently used in standard of care. The three methods being compared are standard stitches and the wound closure devices, Clozex, and Zipline. All of these methods are approved by the FDA.
Detailed Description
There are many surgical wound closure methods commonly used in practice today. These usually involve a combination of braided and monofilament sutures in the subcutaneous fascia and fat as well as the subcuticular layers of the skin. The methods chosen by surgeons vary widely even amongst partners at the same institution for many reasons, including training background and conflicting reports in the literature. In some cases, these closure techniques can be time consuming and associated with increased rates of poor cosmetic outcomes or complications. There have been new wound closure products to reach the market that have been designed (Zipline - Campbell, CA and Clozex - Wellesley, MA), claiming to increase the speed of closure and decrease the rate of complications. These products both utilize an adhesive backed film to adhere to the skin along with a proprietary method to enhance skin apposition to reduce tension during the healing process. There has been no randomized controlled trial to determine superiority of the above listed surgical closure methods compared to traditional methods.
Our study aims to compare a "traditional" wound closure using both braided and monofilament sutures to the newer wound closure systems. By determining which method provides superior results, we will improve patient outcomes and satisfaction. The study also aims to assess health care value by exploring the costs associated with each closure technique. In addition to material expenses associated with the traditional sutures, we seek to explore if there is a significant difference in the time required to perform each wound closure method. Every minute of anesthesia and operating room utilization is associated with costs borne by the patient and the health care system. By finding which closure method is the fastest and associated with the best outcome we can improve healthcare value.
These methods will be tested in a randomized controlled trial and will be analyzed with multivariate statistical analysis to examine statistical significance. Subjects will be randomized in a 1:1:1 fashion to sutures, Closex, or Zipline. Surgeons will complete a satisfaction questionnaire about the randomized method used for closure. Surgical subjects will complete a satisfaction questionnaire at two follow up visits that align with standard of care visits and will have the incision measured and examined. Our primary objective outcome measure will be an assessment of surgical scar dimensions. Our hypothesis is that the 3 study groups will have similar objective scar measurements but that the savings in time associated with the new wound closure methods will be significant.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Incision, Surgical
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Suture
Arm Type
Active Comparator
Arm Description
Standard suture wound closure
Arm Title
Adhesive wound closure device
Arm Type
Active Comparator
Arm Description
Clozex wound closure device
Arm Title
Adhesive wound closure device with zip ties
Arm Type
Active Comparator
Arm Description
Zipline wound closure device
Intervention Type
Device
Intervention Name(s)
Suture
Intervention Description
Standard suture wound closure device.
Intervention Type
Device
Intervention Name(s)
Clozex
Intervention Description
Interlaced adhesive wound closure device.
Intervention Type
Device
Intervention Name(s)
Zipline
Intervention Description
Adhesive wound closure device using zip-tie like strips.
Primary Outcome Measure Information:
Title
Stony Brook Scar Evaluation Scale
Description
Scores range from 0-5. Higher scores indicate better scar healing. Lower scores indicate worse scar healing
Time Frame
2 weeks post-operative
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 18+
Patient scheduled to undergo elective orthopaedic surgical procedure with a minimum anticipated incision length of 3 cm.
Willingness and ability to comply with scheduled visits and study procedures.
Exclusion Criteria:
Revision Surgery
Compromised wound healing (autoimmune disorder, chronic steroids, connective tissue disorder)
Pregnant women, fetuses, neonates, children, prisoners, cognitively impaired, educational or economically disadvantage, non-English speaking subjects.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark Miller, MD
Organizational Affiliation
University of Virginia
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Virginia
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22903
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Individual data will not be share. Group means will be shared.
Citations:
PubMed Identifier
36155955
Citation
Burke JF, MacLean IS, Smith JM, Hart JM, Miller MD. A Prospective, Randomized, Controlled Comparison of Adhesive Wound Closure Devices in an Orthopaedic Patient. J Am Acad Orthop Surg Glob Res Rev. 2022 Sep 23;6(9):e22.00179. doi: 10.5435/JAAOSGlobal-D-22-00179. eCollection 2022 Sep 1.
Results Reference
derived
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Orthopaedic Surgical Wound Closure Comparison Study
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