Post-Operative Cesarean Section Cosmesis
Recruiting
N/A
Interventional Study
Cesarean Delivery
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 44
- Sex
- Female
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 52 (estimated)
- Sponsor
- Wake Forest University Health Sciences · Other
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About This Trial
Given the high numbers of cesarean deliveries being performed today, there has been interest in optimizing surgical techniques. Several recent reviews have summarized the evidence for various steps of cesarean delivery, but surprisingly in many cases there is little scientific evidence on which to base the choice of surgical technique.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age 18-44
* Any race
* Any parity
* Scheduled cesarean section
* Neuraxial analgesia
Exclusion Criteria:
* Non-English Speaking
* Incarcerated
* Maternal Connective Tissue Disorder
* Systemic maternal steroid use
* Three prior cesarean deliveries
* Body Mass Index (BMI) \>40
Contacts