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Cesarean Wound Closure: Dermabond Versus Steri Strips

NCT ID: NCT04621994

Last Updated: 2020-11-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

133 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-11-30

Study Completion Date

2022-07-31

Brief Summary

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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

Detailed Description

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Conditions

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Scar

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Steri Strips Arm

Group Type ACTIVE_COMPARATOR

Steri Strips

Intervention Type OTHER

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

Dermabond Arm

Group Type EXPERIMENTAL

Dermabond

Intervention Type OTHER

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

Interventions

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Dermabond

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

Intervention Type OTHER

Steri Strips

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

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Women age 18-45 who are undergoing planned or unscheduled cesarean section at Regional One Health
* Gestational age \> 24 weeks
* Planned Pfannenstiel incision
* Willing to consent to the study

Exclusion Criteria

* Emergency or urgent cesarean section
* Vertical skin incision
* Intrapartum intraamniotic infection
* Diabetes
* Unwilling to consent to the study
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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University of Tennessee

OTHER

Sponsor Role lead

Responsible Party

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Laura Grese Willingham

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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20-07302-FB

Identifier Type: -

Identifier Source: org_study_id