C.Delivery; Penetration, Pregnant Uterus, by Instrument, Obesity
Conditions
Brief summary
The purpose of this randomized controlled prospective trial is to guide physicians on the most effective evidenced based skin closure during a cesarean section for the obese gravida, defined as a BMI of 40 or greater. The study will compare two closure methods: subcuticular sutures and surgical staples.
Detailed description
The study will screen and attempt to enroll pregnant women admitted to labor and delivery who have a BMI of 40 or greater. The participants will be randomized to receiving skin closure with subcuticular sutures or surgical staples if they undergo cesarean section. Either technique is currently standard of care. Participants who end up undergoing cesarean section will be included in the final data analysis. The participants will be followed for wound complication in the first 6 weeks post operatively. Wound complication will be defined as wound disruption or infection within 6 weeks post operatively. Design and Project Type This study is a randomized controlled trial. At the study facility, in 2012 and 2013, over 300 cesarean sections were performed each year in women with BMI of 40 or greater. Based on this, the investigators expect the duration of the study to be 2 years. Randomization and data collection will be completed on 420 women. Description of Intervention Two interventions will be used in this project: subcuticular suture and surgical staples. The subcuticular suture will be the size and type of suture chosen by the surgeon at the time of cesarean. The surgical staples will be the standard staples used on the labor and delivery unit.
Interventions
PROCEDURERandomizing to Suture or Staple closure of Cesarean section
Randomizing to either surgical subcuticular suture or surgical staples in women of BMI greater than 40 undergoing Cesarean section delivery.
Sponsors
Banner Health
Pediatrix
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No
Inclusion criteria
* Pregnant woman * Time to approach and consent the patient prior to undergoing cesarean delivery * Able to give informed consent, include age 18 or greater and ability to read and understand English * BMI of 40 or greater on most recent hospital documentation * Willingness to participate in the study and ability to read, understand and sign the informed consent document
Exclusion criteria
* Inability to give informed consent, including inability to read and understand English and age under 18 years * Evidence of current skin infection or breakdown at or near the site of surgical incision * Any immune compromised status, including AIDS * Negative pressure wound therapy applied at time of surgery
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Rate of wound complication, comparing the outcomes from the two arms | 2 years | Rate of wound complication comparing the outcomes of subcuticular sutures to surgical staples for cesarean wound closure in the obese gravida during the first 6 weeks postpartum. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Frequency of and risk factors for wound complication after cesarean delivery in the obese gravida. | 2 years | wound complication frequency |
| Type and location of cesarean incisions in the obese gravida. | 2 years | type and location of incisions |
| Effect of medical comorbidities on wound disruption. | 2 years | medical comorbidities on wound disruption |
Countries
United States
Outcome results
None listed