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Post-Operative Cesarean Section Cosmesis

Wake Forest University Health Sciences · NCT06412978

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18–44 · Women only
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
52
US sites recruiting
1
Study start
September 5, 2024
Record last updated
October 23, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Being studied: absorbable subcuticular polyglycolic acid staples (INSORB); subcuticular, polyglecaprone suture (Monocryl)

Conditions: Cesarean Delivery

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full 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

Recruiting US locations

  • Wake Forest University Health Sciences

    Winston-Salem, NC 27157

    Site contact: Christina Tulbert · 336-716-2383 · Christina.Tulbert@Advocatehealth.org

Study contacts (from the official record)

  • Christina Tulbert · 336.716.2383 · Christina.Tulbert@Advocatehealth.org
All pregnancy studies in North Carolina →
Post-Operative Cesarean Section Cosmesis (NCT06412978) | Bored Studies