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Staples Versus Suture for Cesarean Wound Closure (SVS)

Primary Purpose

Wound

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Surgical staples
Absorbable Surgical Suture
Sponsored by
University of Alabama at Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Wound focused on measuring Staples, Sutures, Cesarean Delivery, Wound, Skin Closure, Wound infection, Wound disruption

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • cesarean delivery

Exclusion Criteria:

  • chronic use of immunosuppressive agents ( e.g.po steroids > 2 weeks)
  • significant immune compromising disease (e.g. AIDS, CD4<200)
  • contraindication to standard post operative pain management (acetaminophen, ibuprofen, oxycodone)
  • refusal or inability to give consent

Sites / Locations

  • UAB Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Absorbable Subcuticular Surgical Suture

Surgical staples

Arm Description

Patients in this arm will receive absorbable subcuticular suture for wound closure of cesarean deliveries.

Patients in this arm will receive surgical staples for wound closure.

Outcomes

Primary Outcome Measures

Percent of Subjects With Composite Wound Morbidity.
this outcome measure included a composite of either disruption and/ or infection of the wound at 4 - 6 weeks post partum. The number of subjects experiencing wound disruption and or wound infection at 4 - 6 weeks post delivery was assessed

Secondary Outcome Measures

Composite Cosmesis Score (Stony Brook Scar Evaluation Score - SBSES) Core - SBSES))
The SBSES assessed five scar components: width, height, color, suture marks and overall appearance. Each component was assigned a score of 0 or 1 with a total sum range of 0 (worst) to 5 (best).
Operative Procedure Time.
time for procedure as measured in minutes
Post Operative Pain - 4 - 6 Weeks Post Delivery
the visual analog pain scale was used. The range is 0 to 10 for reporting pain: 0 = no pain and 10 = unbearable distress
Post Operative Pain - 72 - 96 Hours Post Delivery
the visual analog pain scale was used. The range is 0 to 10 for reporting pain: 0 = no pain and 10 = unbearable distress
Subject Reported Satisfaction With Appearance of Scar
Subject reported satisfaction of the scar appearance was assessed by using a scale of 1 - 5 with 1 being worst appearance and 5 being best appearance
Subject Satisfaction With Comfort With Scar
Scar discomfort satisfaction was reported by subject perception using a scale of 1 - 5. A score of 1 would be the worst comfort and a score of 5 would be the best comfort
Subject Satisfaction With Location of Scar
Satisfaction with location of scar was reported by subject using a scale of 1 - 5. A score of 1 would be the worst location of a scar and a score of 5 would be the best location of a scar

Full Information

First Posted
November 4, 2009
Last Updated
September 2, 2014
Sponsor
University of Alabama at Birmingham
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1. Study Identification

Unique Protocol Identification Number
NCT01008449
Brief Title
Staples Versus Suture for Cesarean Wound Closure
Acronym
SVS
Official Title
Surgical Staples vs. Absorbable Subcuticular Suture for Wound Closure of Cesarean Deliveries
Study Type
Interventional

2. Study Status

Record Verification Date
September 2014
Overall Recruitment Status
Terminated
Why Stopped
New studies were reporting that sutures are beneficial, hindering the possibility of enrollment.
Study Start Date
August 2009 (undefined)
Primary Completion Date
February 2011 (Actual)
Study Completion Date
February 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alabama at Birmingham

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The objective of this randomized controlled trial is to compare wound morbidity (including disruption and infection) in surgical staples versus absorbable subcuticular suture for wound closure in cesarean deliveries.
Detailed Description
Cesarean delivery (CD) is a common surgical procedure with over 1 million performed annually in the United States. The rate of CD is steadily increasing. In 2006, an estimated 31.1% of U.S. births were by CD. Approximately two thirds of these are primary procedures and 90% of CD will later undergo a repeat cesarean delivery. The rise in CD has been attributed to changes in physician and patient expectations, attitudes about risk, and changes in clinical practice. These include decreased vaginal birth after cesarean delivery (VBAC), breech vaginal deliveries, and operative vaginal deliveries as well as an increase in maternal request, failed induction of labor, and elective repeat CD. The CD rate is expected to rise as high as 40-50% in the next decade if the increasing trend continues unabated. Despite the large number of CD performed, there is no agreed standard for skin closure. The most commonly used materials are surgical staples and absorbable subcuticular suture. Staples have a clear benefit in decreasing operating time. In theory, staples also have a decreased chance of bacterial migration into the wound, decreased tension at the incision edges, and less damage to capillaries in the subcuticular layer of skin than absorbable subcuticular suture. However, some argue that staples are more painful and have a worse cosmetic appearance. This is especially the case for staples that remain in place longer than recommended and leave "track marks." Staples are also less visually appealing to patients. The Cochrane Collaboration identified one randomized controlled trial (RCT) that addressed skin closure for CD (Alderice, 2003). This study included 66 women and compared absorbable subcuticular suture versus surgical staples for skin closure of CD. Surgical staples had shorter operating time but absorbable subcuticular suture had decreased post-operative pain and better cosmesis at the 6 week post-operative visit (Frishman, 1997). Rousseau, J. presented opposing findings in her RCT "A Randomized Study Comparing Subcuticular Sutures Versus Staples for Skin Closure at Cesarean Sections". In this study, staples had better cosmesis, decreased pain at the post-operative visit, and shorter operating time (Rousseau, 2009). Neither study assessed wound disruption or infection directly. With such widely varying findings and lack of data there is a need to identify the cesarean section skin closure which provides the best outcomes for the most common major surgical procedure in women. We have undertaken a RCT to compare surgical staples vs. absorbable subcuticular suture for the closure of the skin in cesarean sections. Our primary outcome is a composite wound morbidity outcome (including wound disruption or infection). Assuming a baseline wound morbidity of 8%, Power of 80%, and a decrease of wound morbidity to 4%, a sample size of 1,204 will be required. Our secondary outcomes will include cosmesis, post-operative pain, health service use/cost, procedure time, and patient satisfaction. The study was terminated after recruitment of approximately 400 subjects after administrative review (see publication: Figueroa et al. Obstet Gynecol. 2013 Jan;121(1):33-8.)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Wound
Keywords
Staples, Sutures, Cesarean Delivery, Wound, Skin Closure, Wound infection, Wound disruption

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
398 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Absorbable Subcuticular Surgical Suture
Arm Type
Active Comparator
Arm Description
Patients in this arm will receive absorbable subcuticular suture for wound closure of cesarean deliveries.
Arm Title
Surgical staples
Arm Type
Active Comparator
Arm Description
Patients in this arm will receive surgical staples for wound closure.
Intervention Type
Device
Intervention Name(s)
Surgical staples
Other Intervention Name(s)
Proximate Plus MD 35 W, Ethicon Endo-surgery
Intervention Description
Surgical staples will be used once for wound closure.
Intervention Type
Device
Intervention Name(s)
Absorbable Surgical Suture
Other Intervention Name(s)
4-0 Monocryl, Ethicon
Intervention Description
Absorbable surgical suture will be used for subcuticular closure at the time of wound closure for cesarean delivery.
Primary Outcome Measure Information:
Title
Percent of Subjects With Composite Wound Morbidity.
Description
this outcome measure included a composite of either disruption and/ or infection of the wound at 4 - 6 weeks post partum. The number of subjects experiencing wound disruption and or wound infection at 4 - 6 weeks post delivery was assessed
Time Frame
4-6 weeks post partum
Secondary Outcome Measure Information:
Title
Composite Cosmesis Score (Stony Brook Scar Evaluation Score - SBSES) Core - SBSES))
Description
The SBSES assessed five scar components: width, height, color, suture marks and overall appearance. Each component was assigned a score of 0 or 1 with a total sum range of 0 (worst) to 5 (best).
Time Frame
at the end of follow up, 4 - 6 weeks post partum
Title
Operative Procedure Time.
Description
time for procedure as measured in minutes
Time Frame
Intraoperative, at time of intervention.
Title
Post Operative Pain - 4 - 6 Weeks Post Delivery
Description
the visual analog pain scale was used. The range is 0 to 10 for reporting pain: 0 = no pain and 10 = unbearable distress
Time Frame
at end of follow-up, 4 - 6 weeks post partum
Title
Post Operative Pain - 72 - 96 Hours Post Delivery
Description
the visual analog pain scale was used. The range is 0 to 10 for reporting pain: 0 = no pain and 10 = unbearable distress
Time Frame
72 - 96 hours post delivery
Title
Subject Reported Satisfaction With Appearance of Scar
Description
Subject reported satisfaction of the scar appearance was assessed by using a scale of 1 - 5 with 1 being worst appearance and 5 being best appearance
Time Frame
4 - 6 weeks post delivery
Title
Subject Satisfaction With Comfort With Scar
Description
Scar discomfort satisfaction was reported by subject perception using a scale of 1 - 5. A score of 1 would be the worst comfort and a score of 5 would be the best comfort
Time Frame
at end of follow-up, 4 - 6 weeks post partum
Title
Subject Satisfaction With Location of Scar
Description
Satisfaction with location of scar was reported by subject using a scale of 1 - 5. A score of 1 would be the worst location of a scar and a score of 5 would be the best location of a scar
Time Frame
at end of follow-up, 4 - 6 weeks post partum

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: cesarean delivery Exclusion Criteria: chronic use of immunosuppressive agents ( e.g.po steroids > 2 weeks) significant immune compromising disease (e.g. AIDS, CD4<200) contraindication to standard post operative pain management (acetaminophen, ibuprofen, oxycodone) refusal or inability to give consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dana Figueroa, MD
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
UAB Hospital
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35249
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
19254586
Citation
Rousseau JA, Girard K, Turcot-Lemay L, Thomas N. A randomized study comparing skin closure in cesarean sections: staples vs subcuticular sutures. Am J Obstet Gynecol. 2009 Mar;200(3):265.e1-4. doi: 10.1016/j.ajog.2009.01.019.
Results Reference
background
PubMed Identifier
9350017
Citation
Frishman GN, Schwartz T, Hogan JW. Closure of Pfannenstiel skin incisions. Staples vs. subcuticular suture. J Reprod Med. 1997 Oct;42(10):627-30.
Results Reference
background
PubMed Identifier
12804476
Citation
Alderdice F, McKenna D, Dornan J. Techniques and materials for skin closure in caesarean section. Cochrane Database Syst Rev. 2003;(2):CD003577. doi: 10.1002/14651858.CD003577.
Results Reference
background
PubMed Identifier
23262925
Citation
Figueroa D, Jauk VC, Szychowski JM, Garner R, Biggio JR, Andrews WW, Hauth J, Tita AT. Surgical staples compared with subcuticular suture for skin closure after cesarean delivery: a randomized controlled trial. Obstet Gynecol. 2013 Jan;121(1):33-8. doi: 10.1097/aog.0b013e31827a072c. Erratum In: Obstet Gynecol. 2013 May;121(5):1113.
Results Reference
derived
Links:
URL
http://www.ncbi.nlm.nih.gov/pubmed/23262925
Description
Link to study results on PubMed

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Staples Versus Suture for Cesarean Wound Closure

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