Clinical Trials Directory

Trials / Unknown

UnknownNCT04621994

Cesarean Wound Closure: Dermabond Versus Steri Strips

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
133 (estimated)
Sponsor
University of Tennessee · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

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

Interventions

TypeNameDescription
OTHERDermabondDermabond will be applied after subcuticular skin closure in lieu of Steri Strips
OTHERSteri StripsSteri Strips will be applied after subcuticular skin closure as routinely done at our institution

Timeline

Start date
2020-11-01
Primary completion
2021-04-01
Completion
2022-07-01
First posted
2020-11-09
Last updated
2020-11-09

Source: ClinicalTrials.gov record NCT04621994. Inclusion in this directory is not an endorsement.