A Novel Wound Retractor Combining Continuous Irrigation and Barrier Protection Reduces Incisional Contamination and Surgical Site Infection in Colorectal Surgery
Primary Purpose
Colorectal Surgery
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CleanCision Wound Retraction and Protection System
Alexis O Wound Protector
Sponsored by
About this trial
This is an interventional prevention trial for Colorectal Surgery focused on measuring wound irrigation, cleancision, colorectal surgery
Eligibility Criteria
Inclusion Criteria:
- Patients 18 years old and above.
- Elective colorectal surgery with a planned resection including open or laparoscopic surgeries.
- Clean -contaminated, contaminated and dirty wounds per the definition above.
- Patients undergoing Standard of care SSI reduction bundle including Prophylactic AB and mechanical bowel preparation.
- Anticipated incision length of 3-17 cm
Exclusion Criteria:
- Patients younger than 18 years old.
- Patients with a preexisting stoma.
- Patiens with prior laparotomy within 15 days.
- Patients with an active infection or systemic antibiotic therapy within 1 week prior to surgery with the exception of preoperative antimicrobial prophylaxis.
- Emergent/ urgent surgery.
Sites / Locations
- Cleveland Clinic Main CampusRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Alexis O Wound Protector
CleanCision Wound Protector
Arm Description
Participants will undergo standard surgical procedure using the Alexis O wound protector.
Participants will undergo standard surgical procedure using the CleanCision Wound Retraction and Protection System
Outcomes
Primary Outcome Measures
Surgical Site Infection rate
To evaluate the 30 day post-operative SSI rate in patients undergoing elective colorectal surgical procedures after intraoperative usage of Alexis O wound protector vs. CleanCision continuous irrigation wound protector.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03816995
Brief Title
A Novel Wound Retractor Combining Continuous Irrigation and Barrier Protection Reduces Incisional Contamination and Surgical Site Infection in Colorectal Surgery
Official Title
A Novel Wound Retractor Combining Continuous Irrigation and Barrier Protection Reduces Incisional Contamination and Surgical Site Infection in Colorectal Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 12, 2019 (Actual)
Primary Completion Date
December 2026 (Anticipated)
Study Completion Date
June 2027 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Cleveland Clinic
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Surgical site infection (SSI) remains a problem in colorectal surgery. Strategies to reduce the incidence of SSI following colorectal surgery are important to improve overall patient outcomes, reduce healthcare-associated costs and provide value-based healthcare to surgical patients.
Preventing contamination of the wound through the use of barrier wound protectors or intraoperative wound irrigation has shown significant promise individually and is an ongoing focus to reduce wound infections SSI.
Detailed Description
Surgical site infection (SSI) remains a persistent and morbid problem in colorectal surgery with published rates ranging from 7 to 25%. The negative outcomes of SSI are well reported and include a significant increase in morbidity, length of hospital stay, readmissions and healthcare-associated cost. Therefore, strategies to reduce the incidence of SSI following colorectal surgery are important to improve overall patient outcomes, reduce healthcare-associated costs and provide value-based healthcare to surgical patients.
Key to the pathogenesis of SSI is the degree of bacterial contamination of the surgical wound. Preventing contamination of the wound or reducing the bacterial load through the use of barrier wound protectors or intraoperative wound irrigation has shown significant promise individually and is an ongoing strategic focus to reduce wound infections after surgery.
The usage of intraoperative wound irrigation has been shown to significantly reduce the risk of SSI via multiple RTC. A surgical device that combines continuous wound irrigation and barrier protection will have an important SSI prevention advantage.
CleanCision is a recently developed apparatus that serves this purpose and was found to reduce bacterial wound contamination in preclinical and clinical trials.
This study aims to investigate the effect of using CleanCision wound protector on the rates of postoperative Surgical Site Infections in comparison to the current wound protector (Alexis O) being used at our institute.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Surgery
Keywords
wound irrigation, cleancision, colorectal surgery
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
702 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Alexis O Wound Protector
Arm Type
Active Comparator
Arm Description
Participants will undergo standard surgical procedure using the Alexis O wound protector.
Arm Title
CleanCision Wound Protector
Arm Type
Experimental
Arm Description
Participants will undergo standard surgical procedure using the CleanCision Wound Retraction and Protection System
Intervention Type
Device
Intervention Name(s)
CleanCision Wound Retraction and Protection System
Intervention Description
wound retraction and irrigation
Intervention Type
Device
Intervention Name(s)
Alexis O Wound Protector
Intervention Description
wound retraction
Primary Outcome Measure Information:
Title
Surgical Site Infection rate
Description
To evaluate the 30 day post-operative SSI rate in patients undergoing elective colorectal surgical procedures after intraoperative usage of Alexis O wound protector vs. CleanCision continuous irrigation wound protector.
Time Frame
30 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients 18 years old and above.
Elective colorectal surgery with a planned resection including open or laparoscopic surgeries.
Clean -contaminated, contaminated and dirty wounds per the definition above.
Patients undergoing Standard of care SSI reduction bundle including Prophylactic AB and mechanical bowel preparation.
Anticipated incision length of 3-17 cm
Exclusion Criteria:
Patients younger than 18 years old.
Patients with a preexisting stoma.
Patiens with prior laparotomy within 15 days.
Patients with an active infection or systemic antibiotic therapy within 1 week prior to surgery with the exception of preoperative antimicrobial prophylaxis.
Emergent/ urgent surgery.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Holly Renner
Phone
216-299-9529
Email
rennerh@ccf.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Scott Steele, MD
Organizational Affiliation
The Cleveland Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cleveland Clinic Main Campus
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Holly M Renner, BS
Phone
216-299-9529
Email
rennerh@ccf.org
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
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A Novel Wound Retractor Combining Continuous Irrigation and Barrier Protection Reduces Incisional Contamination and Surgical Site Infection in Colorectal Surgery
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