610 Participants NeededMy employer runs this trial

Steri-Strips for Cesarean Section Incisions

(STRIP-CS Trial)

MP
Overseen ByMatthew Perera, DO, MS
Age: 18+
Sex: Female
Trial Phase: Academic
Sponsor: Riverside University Health System Medical Center
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This study is evaluating whether Steri-Strips® provide additional benefits when used after cesarean section (C-section) surgery. Steri-Strips are adhesive strips that are commonly placed over a surgical incision to provide support while the wound heals. At our hospital, Steri-Strips are routinely used after C-sections in addition to standard wound closure techniques, although they are not considered part of the standard recommended closure method.

Researchers want to determine whether adding Steri-Strips actually reduces wound complications such as infection, fluid collection under the skin, or reopening of the incision. Previous studies have shown mixed results, with some suggesting little difference in wound healing outcomes while others reported differences in scar appearance. Steri-Strips may also increase costs, add time to the surgery, and occasionally cause skin irritation or allergic reactions.

Participants in this study will be randomly assigned to one of two groups. One group will receive standard cesarean wound closure with Steri-Strips, while the other group will receive standard wound closure without Steri-Strips. Researchers will compare wound healing, complications, patient outcomes, and costs between the two groups.

The goal of this study is to determine whether Steri-Strips improve recovery after cesarean delivery and whether their routine use is beneficial and cost-effective. The findings may help guide future recommendations for cesarean wound care and improve outcomes for patients undergoing C-section delivery.

Are You a Good Fit for This Trial?

This trial is for people having a cesarean section (C-section) who do not have any specific exclusion criteria listed. Participants must be able to follow study instructions and agree to random assignment of wound closure method.

Inclusion Criteria

I am a woman who is 18 years old or older.
Pregnant patients undergoing cesarean delivery at Riverside University Health System Medical Center (RUHS)
Able and willing to provide informed consent

Exclusion Criteria

I am able and willing to give my consent to join the study.
Known allergy or hypersensitivity to Steri-Strip™ materials or adhesives
Anticipated inability to complete the 30-day postpartum follow-up evaluation

What Are the Treatments Tested in This Trial?

Interventions

  • Steri-Strip™ Skin Closures

Trial Overview

The study compares two ways of closing C-section incisions: standard wound closure alone versus standard closure plus Steri-Strips, which are adhesive strips placed over the incision. Patients are randomly assigned to one group or the other.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Standard Closure + Steri-StripsExperimental Treatment2 Interventions
Group II: Standard Closure AloneActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Riverside University Health System Medical Center

Lead Sponsor

Trials
10
Recruited
19,300+