Skip to content

Staples Versus Suture for Cesarean Wound Closure

Surgical Staples vs. Absorbable Subcuticular Suture for Wound Closure of Cesarean Deliveries

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01008449
Acronym
SVS
Enrollment
398
Registered
2009-11-05
Start date
2009-08-31
Completion date
2011-02-28
Last updated
2014-09-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wound

Keywords

Staples, Sutures, Cesarean Delivery, Wound, Skin Closure, Wound infection, Wound disruption

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.)

Interventions

Surgical staples will be used once for wound closure.

DEVICEAbsorbable Surgical Suture

Absorbable surgical suture will be used for subcuticular closure at the time of wound closure for cesarean delivery.

Sponsors

University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
16 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Percent of Subjects With Composite Wound Morbidity.4-6 weeks post partumthis 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

MeasureTime frameDescription
Operative Procedure Time.Intraoperative, at time of intervention.time for procedure as measured in minutes
Post Operative Pain - 4 - 6 Weeks Post Deliveryat end of follow-up, 4 - 6 weeks post partumthe 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 Delivery72 - 96 hours post deliverythe visual analog pain scale was used. The range is 0 to 10 for reporting pain: 0 = no pain and 10 = unbearable distress
Composite Cosmesis Score (Stony Brook Scar Evaluation Score - SBSES) Core - SBSES))at the end of follow up, 4 - 6 weeks post partumThe 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).
Subject Satisfaction With Comfort With Scarat end of follow-up, 4 - 6 weeks post partumScar 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 Scarat end of follow-up, 4 - 6 weeks post partumSatisfaction 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
Subject Reported Satisfaction With Appearance of Scar4 - 6 weeks post deliverySubject 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

Countries

United States

Participant flow

Participants by arm

ArmCount
Absorbable Subcuticular Surgical Suture
Patients in this arm will receive absorbable subcuticular suture for wound closure of cesarean deliveries. Absorbable Surgical Suture: Absorbable surgical suture will be used for subcuticular closure at the time of wound closure for cesarean delivery.
171
Surgical Staples
Patients in this arm will receive surgical staples for wound closure. Surgical staples: Surgical staples will be used once for wound closure.
179
Total350

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up2919

Baseline characteristics

CharacteristicAbsorbable Subcuticular Surgical SutureSurgical StaplesTotal
Age, Continuous26.9 years
STANDARD_DEVIATION 5.9
26.7 years
STANDARD_DEVIATION 6.1
26.8 years
STANDARD_DEVIATION 6
Region of Enrollment
United States
171 participants179 participants350 participants
Sex: Female, Male
Female
171 Participants179 Participants350 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
12 / 17128 / 179
serious
Total, serious adverse events
0 / 1710 / 179

Outcome results

Primary

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

Time frame: 4-6 weeks post partum

ArmMeasureValue (NUMBER)
Absorbable Subcuticular Surgical SuturePercent of Subjects With Composite Wound Morbidity.5.9 percentage of subjects
Surgical StaplesPercent of Subjects With Composite Wound Morbidity.14.5 percentage of subjects
Secondary

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).

Time frame: at the end of follow up, 4 - 6 weeks post partum

ArmMeasureValue (MEDIAN)
Absorbable Subcuticular Surgical SutureComposite Cosmesis Score (Stony Brook Scar Evaluation Score - SBSES) Core - SBSES))4 units on a scale
Surgical StaplesComposite Cosmesis Score (Stony Brook Scar Evaluation Score - SBSES) Core - SBSES))3 units on a scale
Secondary

Operative Procedure Time.

time for procedure as measured in minutes

Time frame: Intraoperative, at time of intervention.

ArmMeasureValue (MEDIAN)
Absorbable Subcuticular Surgical SutureOperative Procedure Time.40 minutes
Surgical StaplesOperative Procedure Time.37 minutes
Secondary

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

Time frame: at end of follow-up, 4 - 6 weeks post partum

ArmMeasureValue (MEDIAN)
Absorbable Subcuticular Surgical SuturePost Operative Pain - 4 - 6 Weeks Post Delivery0 units on a scale
Surgical StaplesPost Operative Pain - 4 - 6 Weeks Post Delivery0 units on a scale
Secondary

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

Time frame: 72 - 96 hours post delivery

ArmMeasureValue (MEDIAN)
Absorbable Subcuticular Surgical SuturePost Operative Pain - 72 - 96 Hours Post Delivery5 units on a scale
Surgical StaplesPost Operative Pain - 72 - 96 Hours Post Delivery5 units on a scale
Secondary

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

Time frame: 4 - 6 weeks post delivery

ArmMeasureValue (MEDIAN)
Absorbable Subcuticular Surgical SutureSubject Reported Satisfaction With Appearance of Scar4 units on a scale
Surgical StaplesSubject Reported Satisfaction With Appearance of Scar4 units on a scale
Secondary

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

Time frame: at end of follow-up, 4 - 6 weeks post partum

ArmMeasureValue (MEDIAN)
Absorbable Subcuticular Surgical SutureSubject Satisfaction With Comfort With Scar4 units on a scale
Surgical StaplesSubject Satisfaction With Comfort With Scar4 units on a scale
Secondary

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

Time frame: at end of follow-up, 4 - 6 weeks post partum

ArmMeasureValue (MEDIAN)
Absorbable Subcuticular Surgical SutureSubject Satisfaction With Location of Scar4 units on a scale
Surgical StaplesSubject Satisfaction With Location of Scar4 units on a scale

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026