Cesarean Wound Closure: Dermabond Versus Steri Strips

NCT04621994 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 133

Last updated 2020-11-09

No results posted yet for this study

Summary

The purpose of this study is to determine overall patient satisfaction with their cesarean section scar with application of Steri-strips vs. Dermabond following subcuticular skin closure of pfannenstiel incision

Conditions

  • Scar

Interventions

OTHER

Dermabond

Dermabond will be applied after subcuticular skin closure in lieu of Steri Strips

OTHER

Steri Strips

Steri Strips will be applied after subcuticular skin closure as routinely done at our institution

Sponsors & Collaborators

  • University of Tennessee

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-11-30
Primary Completion
2021-04-30
Completion
2022-07-31

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04621994 on ClinicalTrials.gov