MedPath

Secondary Versus Tertiary Wound Closure in High Risk Gynecologic Abdominal Surgical Incisions

Not Applicable
Terminated
Conditions
Surgical Incision
Interventions
Procedure: Historical Wound Closure
Procedure: Tertiary Wound Closure
Registration Number
NCT03861065
Lead Sponsor
Wake Forest University Health Sciences
Brief Summary

The purpose of this research study is to determine if closing a surgical wound differently is better than the procedure that is currently used. The wound will be closed with what is considered "tertiary intent." This means, rather than leaving the wound open, the wound will be partially closed after surgery, and then completely closed 4-7 days after surgery. The investigators also want to see how this new wound closure process affects your quality of life.

Detailed Description

Primary Objective

To compare the percentage of patients whose wound remained closed on postoperative day #30 after tertiary closure compared to historical controls who underwent secondary would closure. We are primarily looking at time to wound closure. We will be able to abstract this information from the postoperative clinic visit notes from patients in the "historical control" cohort. We will identify 20 patients with characteristics described in the inclusion criteria of this study who underwent laparotomy with secondary would closure during the calendar year 2018.

Secondary Objectives

To compare the proportion of acute and chronic wound infection in wounds closed with a tertiary closure technique to historical controls receiving a secondary wound closure.

To compare the length of stay of patients receiving a tertiary wound closure to historical controls receiving a secondary wound closure.

To describe the number of patients receiving a tertiary wound closure that return within 30 days of surgery as compared to historical controls receiving a secondary wound closure.

To describe the quality of life in patients receiving a tertiary wound closure.

Recruitment & Eligibility

Status
TERMINATED
Sex
Female
Target Recruitment
8
Inclusion Criteria
  • Patients with high risk class II, class III, class IV abdominal wounds
  • Undergoing laparotomy for gynecologic related disorders
  • Patients undergoing laparotomy for both benign and malignant diagnoses will be included in this study
Read More
Exclusion Criteria
  • Pregnancy
  • Allergy to triclosan
  • Patients undergoing HIPEC
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Historical Wound ClosureHistorical Wound ClosureThe standard approach to your wound would be to leave it partially open and let it heal over a period of 3-6 months ("secondary closure").
Tertiary Wound ClosureTertiary Wound ClosureIn the alternative tertiary wound closure, the wound will be partially closed rather than being left open. Sutures in the skin will be placed but not closed. A vacuum assisted closure device will be placed over the wound to help healing. After 4-7 days, the vacuum device will be removed, and the participant's doctor will close the wound.
Primary Outcome Measures
NameTimeMethod
Percentage Comparisons of Tertiary Wound Closure Versus Historical Controls Postoperative Day 3030 days after tertiary wound closure

The percent of wound closure that occurs postoperative day #30 after tertiary wound closure as compared to historical controls receiving a secondary wound closure.

Secondary Outcome Measures
NameTimeMethod
Proportions of Tertiary Technique Versus Historical Controls30 days after tertiary wound closure

The proportion of SSI using a tertiary closure technique compared to historical controls receiving a secondary would closure.

Length of Hospital StayUp to 3 months after surgery

The length of stay as defined by the time from surgery to discharge as compared to historical controls receiving a secondary would closure.

Proportion of Patients Returning after SurgeryUp to 30 days after surgery

The proportion of patients that return within 30 days of surgery.

Change of Quality of Life Questionnaire SF-36Up to 3 months after tertiary wound closure

The quality of life in patients receiving a tertiary wound closure. The scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability.

Trial Locations

Locations (1)

Comprehensive Cancer Center of Wake Forest University

🇺🇸

Winston-Salem, North Carolina, United States

© Copyright 2025. All Rights Reserved by MedPath