PRIC: Application of PREVENA in Reducing Surgical Site Complications Following Reversal of Ileostomy or Colostomy
Study Details
Study Description
Brief Summary
Surgical site infections (SSI) remain one of the most common complications associated with reversal of ileostomy and colostomy. In addition to having detrimental impacts on the patient's post-operative course, they also pose significant financial ramifications.
There have been comparative studies in the use of negative pressure wound therapy in reducing surgical site infections.
PREVENA Incision Management System is a type of disposable, customizable and powered negative pressure system designed to help manage and protect surgical incisions and their surrounding environment. It is now commonly used as a surgical wound dressings in the setting of vascular surgeries, post-cesarean infections and colorectal resections.
Our study is designed as a randomised controlled trial to examine if PREVERA therapy as a NPWT is more superior than conventional dressings in reducing the rate of surgical site infections.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Background:
Surgical site infections (SSI) remain one of the most common complications associated with reversal of ileostomy. In addition to having detrimental impacts on the patient's post-operative course, they also pose significant financial ramifications.
The use of Negative Pressure Wound Therapy (NPWT) is one strategy that has been extensively studied in reducing the rate of surgical site infections.
PREVENA Therapy is a form of Incisional Negative Pressure Wound Therapy (INPWT) that has been widely used in the management of closed surgical incisions. They are delivered as prophylactic measures in preventing surgical complications such as surgical site infections.
Trial Design:
This study is designed as a randomized, controlled, open-label, multi-center superiority trial with 2 parallel groups and primary endpoint of surgical site infection at day 7 (after 7-day use of PREVENA) and day 30.
Study Setting The trial will be conducted at two different hospitals located in Dublin, Ireland: St James Hospital - Ireland's largest acute academic teaching hospital (Academic Partner - Trinity College Dublin); Tallaght University Hospital - (Academic Partner - Trinity College Dublin)
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Patients applied with PREVENA system This arm relates to the group of participants applied with PREVANA system post reversal of colostomy/ileostomy. |
Device: PREVENA Incision Management System
Eligible participants, i.e. participants meeting inclusive criteria, will be randomised in equal proportions and divided into two arms. The PREVENA dressings will be applied to the
Other Names:
|
| No Intervention: Patients applied with conventional dressings This arm relates to the group of participants applied with conventional dressings post reversal of colostomy/ileostomy |
Outcome Measures
Primary Outcome Measures
- To measure surgical site infection incidence on outpatient follow up post reversal ileostomy/colostomy [Four to Six weeks]
The investigators will be assessing and measuring the incidence of surgical site incidence on follow up appointments
Secondary Outcome Measures
- To measure surgical site infection incidence on day 5 post reversal ileostomy/colostomy (or earlier, if deemed fit for discharge prior to day 5) [Five days post reversal ileostomy/colostomy]
The investigators will be assessing and measuring the incidence of surgical site incidence on day 5 post reversal ileostomy/colostomy
- To measure the time to wound healing [One to Four weeks]
The investigators will be assessing and measuring the time to wound healing based on the duration and last appointment date of home visits by public healthcare nurses involving wound care management
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Patients aged over 18 years old
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Patients undergoing elective reversal of ileostomy/colostomy
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Patients who agree to consent to inclusion and follow-up protocol
Exclusion Criteria:
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Patients who do not fulfil study protocol
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Dressings being removed outside defined time periods
-
Patients who do not attend for regular outpatient follow up appointments
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | St James's Hospital | Dublin | Ireland | D08 NHY1 |
Sponsors and Collaborators
- St. James's Hospital, Ireland
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- St James Hospital