DACC in the REduction of Surgical Site INfection (DRESSINg)
Primary Purpose
Infection, Bacterial, Wound Infection, Wound Infection, Surgical
Status
Recruiting
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
DACC-Coated Post Operative Dressing
Sponsored by
About this trial
This is an interventional treatment trial for Infection, Bacterial focused on measuring Infection, Surgical Site Infection, Dialkylcarbamoylchloride
Eligibility Criteria
Inclusion Criteria:
In order to be eligible for inclusion in the study the participants must meet the following criteria:
- Adults ≥18 yrs undergoing clean or clean-contaminated lower limb vascular surgery, with wounds closed by primary intention.
- Able to understand the Patient Information Sheet and supplementary materials and capable and willing to give informed consent and follow the protocol requirements (including attending all follow-up visits and completing written questionnaires).
Exclusion Criteria:
Patients will not be included in the study if they meet any of the following exclusion criteria:
- Patients on antibiotics for other conditions at the time of surgery or in the follow up period.
- Patients undergoing any procedure that does not include lower limb incisions.
- Allergies to any component of either the DACC-coated dressing or the control dressing.
- Inability to give informed consent due to incapacity (as defined by the MCA 2005)
- Aged under 18 years at the time of recruitment
- Use of investigational drug/device therapy within preceding 4 weeks that may interfere with this study.
Sites / Locations
- Academic Vascular Surgery Unit, Vascular Laboratory, Alderson House, Hull Royal InfirmaryRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
DACC-Coated Post-Operative Dressing
Non-DACC coated Occlusive Post-operative Film Dressing
Arm Description
DACC-Coated Post-Operative Dressing
Non-DACC coated Occlusive Post-operative Film Dressing
Outcomes
Primary Outcome Measures
30 day infection rate
Surgical Site Infection at 30 days post-op
Secondary Outcome Measures
1 year infection rate
Surgical Site Infection at 1 year post-op (implant patients only)
Quality of Life (SF-36 V2)
Quality of Life (EQ-5D-5L)
Mortality
30-day mortality
Bluebelle wound healing questionnaire
Full Information
NCT ID
NCT02992951
First Posted
December 12, 2016
Last Updated
February 1, 2023
Sponsor
Hull University Teaching Hospitals NHS Trust
Collaborators
University of Hull
1. Study Identification
Unique Protocol Identification Number
NCT02992951
Brief Title
DACC in the REduction of Surgical Site INfection
Acronym
DRESSINg
Official Title
A Randomised Controlled Trial to Assess the Clinical and Cost Effectiveness of Dialkylcarbamoylchloride (DACC) Coated Post-operative Dressings Versus Standard Care in the Prevention of Surgical Site Infection in Clean or Clean-contaminated, Vascular Surgery.
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 19, 2017 (Actual)
Primary Completion Date
January 1, 2025 (Anticipated)
Study Completion Date
January 1, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hull University Teaching Hospitals NHS Trust
Collaborators
University of Hull
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Surgical site infection is an infection at a place in the body where surgery has taken place, and has been reported in around 5% of people undergoing an operation. In vascular surgery, infection rates are as high as 30%. Methods to reduce this rate of infection should be investigated thoroughly for their effectiveness and cost-effectiveness.
The investigators aim to conduct a research trial examining one such method. Leukomed Sorbact is a wound dressing coated with a chemical (DACC) derived from spider-silk that interacts with, and binds bacteria, causing them to be mechanically removed from a wound when the dressing is changed.The trial aims to compare the effectiveness of this dressing to a standard, non-coated dressing, in the reduction of surgical site infection.
718 patients from a number of centres across the UK will be recruited to this study. Adult patients who are having a vascular surgery operation will be approached for entry into the trial. The trial will be explained to them, as well as an explanation that participation is voluntary and their operation or other aspects of their care will not be impacted in any way should participants not wish to participate.
Participants will be randomised by computer into one of two groups - one group whose wounds are dressed with Leukomed Sorbact, and the other whose wounds are dressed with a standard dressing. Patients will be followed up at 5-7 days and 30 days, and at 1 year. At the follow up, their wounds will be inspected for infection, and participants will be asked to complete short questionnaires measuring quality of life.
The trial will aim to answer a number of questions, with the primary question being does a DACC coated dressing applied after an operation reduce the risk of an infection at the surgery site? It will also ask whether this treatment is cost-effective and whether it promotes satisfactory healing.
A Study Within a Trial will validate a remote diagnostic measure for detecting surgical site infection using wound images and the Bluebelle Wound Healing Questionnaire.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infection, Bacterial, Wound Infection, Wound Infection, Surgical, Surgical Incision, Surgical Wound
Keywords
Infection, Surgical Site Infection, Dialkylcarbamoylchloride
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
718 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
DACC-Coated Post-Operative Dressing
Arm Type
Experimental
Arm Description
DACC-Coated Post-Operative Dressing
Arm Title
Non-DACC coated Occlusive Post-operative Film Dressing
Arm Type
No Intervention
Arm Description
Non-DACC coated Occlusive Post-operative Film Dressing
Intervention Type
Device
Intervention Name(s)
DACC-Coated Post Operative Dressing
Other Intervention Name(s)
Leukomed Sorbact
Intervention Description
Leukomed Sorbact is a non-active coated wound dressing, containing Dialkylcarbomoylchloride. This is a bacteria-binding compound that adheres bacteria via hydrophobic interaction and removes them from the wound bed at dressing change.
Primary Outcome Measure Information:
Title
30 day infection rate
Description
Surgical Site Infection at 30 days post-op
Time Frame
30 days
Secondary Outcome Measure Information:
Title
1 year infection rate
Description
Surgical Site Infection at 1 year post-op (implant patients only)
Time Frame
1 year
Title
Quality of Life (SF-36 V2)
Time Frame
7 days, 30 days, 3 months, 6 months, 1 year
Title
Quality of Life (EQ-5D-5L)
Time Frame
7 days, 30 days, 3 months, 6 months, 1 year
Title
Mortality
Description
30-day mortality
Time Frame
30 days
Title
Bluebelle wound healing questionnaire
Time Frame
Days 30 and 37
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
In order to be eligible for inclusion in the study the participants must meet the following criteria:
Adults ≥18 yrs undergoing clean or clean-contaminated lower limb vascular surgery, with wounds closed by primary intention.
Able to understand the Patient Information Sheet and supplementary materials and capable and willing to give informed consent and follow the protocol requirements (including attending all follow-up visits and completing written questionnaires).
Exclusion Criteria:
Patients will not be included in the study if they meet any of the following exclusion criteria:
Patients on antibiotics for other conditions at the time of surgery or in the follow up period.
Patients undergoing any procedure that does not include lower limb incisions.
Allergies to any component of either the DACC-coated dressing or the control dressing.
Inability to give informed consent due to incapacity (as defined by the MCA 2005)
Aged under 18 years at the time of recruitment
Use of investigational drug/device therapy within preceding 4 weeks that may interfere with this study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ross Lathan, MBBS
Phone
01482674643
Email
ross.lathan2@nhs.net
First Name & Middle Initial & Last Name or Official Title & Degree
Judith Long
Phone
01482 675784
Email
judith.long2@nhs.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
George Smith, M.D
Organizational Affiliation
Hull and East Yorkshire NHS Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Academic Vascular Surgery Unit, Vascular Laboratory, Alderson House, Hull Royal Infirmary
City
Hull
State/Province
East Riding Of Yorkshire
ZIP/Postal Code
HU3 2JZ
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ross Lathan, MbChB
Phone
01482674643
Email
ross.lathan2@nhs.net
First Name & Middle Initial & Last Name & Degree
George E Smith, M.D.
First Name & Middle Initial & Last Name & Degree
Ian C Chetter, M.D
First Name & Middle Initial & Last Name & Degree
Joshua P Totty, MBBS
First Name & Middle Initial & Last Name & Degree
Paris L Cai, MbChB
First Name & Middle Initial & Last Name & Degree
Ross Lathan, MbChB
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30680225
Citation
Totty JP, Harwood AE, Cai PL, Hitchman LH, Smith GE, Chetter IC. Assessing the effectiveness of dialkylcarbamoylchloride (DACC)-coated post-operative dressings versus standard care in the prevention of surgical site infection in clean or clean-contaminated, vascular surgery (the DRESSINg trial): study protocol for a pilot feasibility randomised controlled trial. Pilot Feasibility Stud. 2019 Jan 18;5:11. doi: 10.1186/s40814-019-0400-2. eCollection 2019.
Results Reference
background
Links:
URL
https://pilotfeasibilitystudies.biomedcentral.com/articles/10.1186/s40814-019-0400-2
Description
Abstract Link
Learn more about this trial
DACC in the REduction of Surgical Site INfection
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