Early Versus Delayed Skin Staple Removal Following Cesarean Delivery in the Obese Patient
Primary Purpose
Wound Complications, Obesity
Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Removal of surgical skin staples
Sponsored by

About this trial
This is an interventional treatment trial for Wound Complications focused on measuring Cesarean delivery, Obesity, Skin staples, Wound complications
Eligibility Criteria
Inclusion Criteria:
- Cesarean delivery
- Body Mass Index ≥ 30 kg/m2
- Transverse (Pfannenstiel or Joel-Cohen) skin incision
- Subcutaneous wound depth ≥ 2 cm
- Surgical staple skin closure
Exclusion Criteria:
- Vertical skin incision
- Non-staple skin closure
- Wound complication (superficial dehiscence, abscess, seroma, hematoma, cellulitis)
- Any complication necessitating prolonged hospitalization
Sites / Locations
- Greenville Memorial Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Early Staple Removal
Delayed Staple Removal
Arm Description
Skin staple removal on post-operative day #3
Skin staple removal on post-operative day 7-10
Outcomes
Primary Outcome Measures
Number of participants with a superficial wound disruption as a measure of efficacy.
Any separation of the wound edge measuring greater than 1 cm that occurs from the time of staple placement to final wound assessment which occurs at 7-10 days after surgery.
Secondary Outcome Measures
Number of participants who develop a wound seroma.
A collection of fluid within the subcutaneous fatty tissue layer.
Number of participants who develop a hematoma of the wound.
A collection of clotted blood within the subcutaneous tissues.
Number of participants who develop a surgical site infection
Infection involving only skin or subcutaneous tissue of the incision which occurs within 30 days after the operation.
Frequency of Visual Analogue Pain Score
Patient rating of pain on a 1-10 scale as assessed at the 7-10 day postoperative visit.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01114451
Brief Title
Early Versus Delayed Skin Staple Removal Following Cesarean Delivery in the Obese Patient
Official Title
A Randomized Controlled Trial of Early Versus Delayed Skin Staple Removal Following Cesarean Delivery in the Obese Patient
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Terminated
Why Stopped
Funding limits exceeded prior to complete enrollment.
Study Start Date
October 2009 (undefined)
Primary Completion Date
November 2011 (Actual)
Study Completion Date
February 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Prisma Health-Upstate
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Whenever a person has a cesarean section there is a risk that there will be a problem with healing of the wound. The most common type of wound healing problem is separation and opening of the skin and fatty tissue just beneath the skin. This type of wound healing problem happens more often when the patient has a high body weight. In most cases, metal staples are used to bring the skin together to close the wound. Usually, the staples are left in place for a longer time when the woman is heavy, in hopes of decreasing the chance of wound healing problems. But it is not known if leaving the staples in for a longer time is actually helpful. In some cases, leaving the staples in longer may cause more pain and will require you to see the doctor again to get the staples taken out. The purpose of this study is to see if there is any difference in how the wound heals in heavy women after cesarean section when the skin staples are removed after a short period of time versus a long period of time.
Detailed Description
Cesarean delivery in the obese gravida is associated with numerous perioperative risks, the most frequent of which is postoperative wound disruption, with a mean incidence of 15%. With the exception of closure of the subcutaneous adipose layer, other useful measures to decrease wound complications in the obese gravida have either not been studied or lack sufficient evidence upon which to base a recommendation.
One such intervention is the delayed removal of surgical skin staples. Skin staplers, which were first introduced in the 1980's, were "grandfathered" through the United States Food and Drug Administration (FDA) approval process, and have since become a widely utilized technique for skin closure. Although neither the FDA nor device manufacturers make a specific recommendation, skin staples are commonly left in situ anywhere from 3 - 10 days.
The physiologic rationale for delayed staple removal is unclear. Wound healing involves four main stages including hemostasis, inflammation, granulation, and remodeling. Each phase can be further broken down into overlapping steps. Reapproximation of the skin edges with staples enables epithelialization, resulting in wound closure by a thin layer of cells by 48 hours post-operatively. Although overall wound healing appears to be delayed in the setting of obesity, whether the specific process of epithelialization is affected is unknown. Therefore, there may not be a physiologic basis for delaying staple removal in obese women.
Furthermore, delayed staple removal has potentially negative effects on patient care that may not be balanced by clinical benefits. Delayed staple removal may be associated with prolongation of patient discomfort, additional clinical visits and increased associated costs. These issues caused us to question whether the practice of delayed skin staple removal in obese women is warranted.
Therefore, this clinical trial is designed to compare wound healing outcomes after cesarean following early (postoperative day #3) versus delayed (postoperative day #7 - 10) skin staple removal in the obese patient.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Wound Complications, Obesity
Keywords
Cesarean delivery, Obesity, Skin staples, Wound complications
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
292 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Early Staple Removal
Arm Type
Experimental
Arm Description
Skin staple removal on post-operative day #3
Arm Title
Delayed Staple Removal
Arm Type
Experimental
Arm Description
Skin staple removal on post-operative day 7-10
Intervention Type
Procedure
Intervention Name(s)
Removal of surgical skin staples
Intervention Description
Skin staples will be removed using standard technique with subsequent placement of steri-trips
Primary Outcome Measure Information:
Title
Number of participants with a superficial wound disruption as a measure of efficacy.
Description
Any separation of the wound edge measuring greater than 1 cm that occurs from the time of staple placement to final wound assessment which occurs at 7-10 days after surgery.
Time Frame
7-10 days after surgery
Secondary Outcome Measure Information:
Title
Number of participants who develop a wound seroma.
Description
A collection of fluid within the subcutaneous fatty tissue layer.
Time Frame
6 weeks after surgery
Title
Number of participants who develop a hematoma of the wound.
Description
A collection of clotted blood within the subcutaneous tissues.
Time Frame
6 weeks after surgery
Title
Number of participants who develop a surgical site infection
Description
Infection involving only skin or subcutaneous tissue of the incision which occurs within 30 days after the operation.
Time Frame
6 weeks after surgery
Title
Frequency of Visual Analogue Pain Score
Description
Patient rating of pain on a 1-10 scale as assessed at the 7-10 day postoperative visit.
Time Frame
7-10 days after surgery
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
52 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Cesarean delivery
Body Mass Index ≥ 30 kg/m2
Transverse (Pfannenstiel or Joel-Cohen) skin incision
Subcutaneous wound depth ≥ 2 cm
Surgical staple skin closure
Exclusion Criteria:
Vertical skin incision
Non-staple skin closure
Wound complication (superficial dehiscence, abscess, seroma, hematoma, cellulitis)
Any complication necessitating prolonged hospitalization
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francis S Nuthalapaty, MD
Organizational Affiliation
Prisma Health-Upstate
Official's Role
Principal Investigator
Facility Information:
Facility Name
Greenville Memorial Hospital
City
Greenville
State/Province
South Carolina
ZIP/Postal Code
29605
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
15596944
Citation
Nuthalapaty FS, Rouse DJ. The impact of obesity on obstetrical practice and outcome. Clin Obstet Gynecol. 2004 Dec;47(4):898-913; discussion 980-1. doi: 10.1097/01.grf.0000135358.34673.48. No abstract available.
Results Reference
background
PubMed Identifier
15995563
Citation
Sarsam SE, Elliott JP, Lam GK. Management of wound complications from cesarean delivery. Obstet Gynecol Surv. 2005 Jul;60(7):462-73. doi: 10.1097/01.ogx.0000166603.43959.aa.
Results Reference
background
PubMed Identifier
16260200
Citation
Berghella V, Baxter JK, Chauhan SP. Evidence-based surgery for cesarean delivery. Am J Obstet Gynecol. 2005 Nov;193(5):1607-17. doi: 10.1016/j.ajog.2005.03.063.
Results Reference
background
PubMed Identifier
16135613
Citation
American College of Obstetricians and Gynecologists. ACOG Committee Opinion number 315, September 2005. Obesity in pregnancy. Obstet Gynecol. 2005 Sep;106(3):671-5. doi: 10.1097/00006250-200509000-00054.
Results Reference
background
PubMed Identifier
19155915
Citation
Walsh C, Scaife C, Hopf H. Prevention and management of surgical site infections in morbidly obese women. Obstet Gynecol. 2009 Feb;113(2 Pt 1):411-5. doi: 10.1097/AOG.0b013e3181945625. No abstract available.
Results Reference
background
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Early Versus Delayed Skin Staple Removal Following Cesarean Delivery in the Obese Patient
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