Total Occlusive Ionic Silver-containing Dressing vs Mupirocin Ointment Application vs Conventional Dressing in Elective Colorectal Surgery: Effect on Incisional Surgical Site Infection
Primary Purpose
Incisional Surgical Site Infections
Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
ionic silver-containing dressing
Mupirocin ointment application
Sponsored by
About this trial
This is an interventional prevention trial for Incisional Surgical Site Infections
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of colorectal neoplasms and plans to undergo an elective surgery with curative aims.
- Open surgical approach
Exclusion Criteria:
- Anastomotic leak
- Mortality
- Lost to follow-up
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
No Intervention
Arm Label
ionic silver-containing dressing
Mupirocin ointment application
Conventional dressing
Arm Description
After placing the staples, a ionic silver-containing dressing was placed covering the wound.
After placing the staples, a Mupirocin ointment application was placed covering the wound.
After placing the staples, a conventional dressing, without application of any special gauze or ointment, was placed covering the wound
Outcomes
Primary Outcome Measures
Incisional Surgical site infection
Secondary Outcome Measures
Full Information
NCT ID
NCT02267122
First Posted
October 14, 2014
Last Updated
October 16, 2014
Sponsor
Hospital General Universitario Elche
1. Study Identification
Unique Protocol Identification Number
NCT02267122
Brief Title
Total Occlusive Ionic Silver-containing Dressing vs Mupirocin Ointment Application vs Conventional Dressing in Elective Colorectal Surgery: Effect on Incisional Surgical Site Infection
Official Title
Total Occlusive Ionic Silver-containing Dressing vs Mupirocin Ointment Application vs Conventional Dressing in Elective Colorectal Surgery: Effect on Incisional Surgical Site Infection
Study Type
Interventional
2. Study Status
Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
January 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital General Universitario Elche
4. Oversight
5. Study Description
Brief Summary
The patients were randomized into 3 groups: those patients undergoing a ionic silver-containing dressing (ISD) (Group 1), those undergoing a Mupirocin ointment application (MOA) (Group 2) and those using a conventional dressing (Group 3) in the surgical wound after finishing an elective colorectal surgery.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Incisional Surgical Site Infections
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
147 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ionic silver-containing dressing
Arm Type
Experimental
Arm Description
After placing the staples, a ionic silver-containing dressing was placed covering the wound.
Arm Title
Mupirocin ointment application
Arm Type
Experimental
Arm Description
After placing the staples, a Mupirocin ointment application was placed covering the wound.
Arm Title
Conventional dressing
Arm Type
No Intervention
Arm Description
After placing the staples, a conventional dressing, without application of any special gauze or ointment, was placed covering the wound
Intervention Type
Procedure
Intervention Name(s)
ionic silver-containing dressing
Intervention Description
After placing the staples, a ionic silver-containing dressing was placed covering the wound
Intervention Type
Procedure
Intervention Name(s)
Mupirocin ointment application
Intervention Description
After placing the staples, Mupirocin ointment application over the wound was performed
Primary Outcome Measure Information:
Title
Incisional Surgical site infection
Time Frame
30 postoperative days
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of colorectal neoplasms and plans to undergo an elective surgery with curative aims.
Open surgical approach
Exclusion Criteria:
Anastomotic leak
Mortality
Lost to follow-up
12. IPD Sharing Statement
Citations:
PubMed Identifier
26206641
Citation
Ruiz-Tovar J, Llavero C, Morales V, Gamallo C. Total Occlusive Ionic Silver-Containing Dressing vs Mupirocin Ointment Application vs Conventional Dressing in Elective Colorectal Surgery: Effect on Incisional Surgical Site Infection. J Am Coll Surg. 2015 Aug;221(2):424-9. doi: 10.1016/j.jamcollsurg.2015.04.019. Epub 2015 Apr 28.
Results Reference
derived
Learn more about this trial
Total Occlusive Ionic Silver-containing Dressing vs Mupirocin Ointment Application vs Conventional Dressing in Elective Colorectal Surgery: Effect on Incisional Surgical Site Infection
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