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RCT on NPWT for Incisions Following Major Lower-limb Amputation to Reduce Surgical Site Infection

Primary Purpose

Amputation Wound, Amputation Stump Complication, Amputation Stump; Infection

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Negative pressure wound therapy
Standard dressing
Sponsored by
London Health Sciences Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Amputation Wound

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • any patient 18 years or older undergoing amputation of the lower limb, either an above knee amputation (AKA) or below knee amputation (BKA)
  • ability to read and write English to undergo informed consent

Exclusion Criteria:

  • patients in which a complete seal cannot be obtained at the time of vacuum placement
  • wounds that are not closed primarily
  • existing infection
  • patient is anticipated to not follow-up
  • inability to read and write English

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Other

    Arm Label

    Negative pressure wound therapy

    Standard dressing

    Arm Description

    A vacuum assisted closure device will be applied in this arm

    Standard dressing will be applied to this arm

    Outcomes

    Primary Outcome Measures

    Surgical site infection
    Surgical site infection will be defined using the Centre for Disease Control and Prevention Guidelines.

    Secondary Outcome Measures

    Length of stay
    length of hospital stay
    Antibiotic use
    requirement for antibiotics to treat surgical site infection
    Reoperation
    requirement for revision of amputation
    Death
    mortality

    Full Information

    First Posted
    May 5, 2017
    Last Updated
    December 6, 2017
    Sponsor
    London Health Sciences Centre
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03144726
    Brief Title
    RCT on NPWT for Incisions Following Major Lower-limb Amputation to Reduce Surgical Site Infection
    Official Title
    Single Center Prospective Randomized Control Trial on Negative Pressure Wound Therapy for Incisions Following Major Lower-limb Amputation to Reduce Surgical Site Infection
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2017
    Overall Recruitment Status
    Unknown status
    Study Start Date
    March 2018 (Anticipated)
    Primary Completion Date
    July 2019 (Anticipated)
    Study Completion Date
    July 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    London Health Sciences Centre

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Surgical site infections following lower extremity amputations have been reported in up to 40% of patients. Surgical site infections have significant morbidity and even mortality in terms of emergency room visits, length of hospital stay, reamputation rates and death. Since its introduction, negative pressure wound therapy has been demonstrated to promote wound healing and possibly decreasing the need for future amputations. The aim of the study is to provide level I evidence for the use of negative pressure wound therapy devices in patients undergoing lower extremity amputation.
    Detailed Description
    Amputations are common vascular surgery procedures performed on patients with multiple medical comorbidities. Historically, morbidity and mortality following major amputation of the lower extremity in this patient population has been high. Recent studies have cited 30-day mortality rates ranging from 6% to 17%, with greater risk among patients with transfemoral vs transtibial amputation. Postoperative goals after amputation include uncomplicated wound healing and, for appropriate candidates, progression to use of a prosthesis for ambulation or transfer. Perioperative wound complications can be devastating in this already debilitated population and can range from 13% to 40%. Postoperative wound complications, such as infection, dehiscence, and formation of haematoma or seroma, are common complications of surgical procedures; particularly among patients with risk factors such as obesity and diabetes. Wound complications may delay recovery, increase patient discomfort and reduce overall quality of life. Increased healthcare costs may be incurred due to prolonged inpatient stay, repeat surgery and the need for increased follow-up. Wounds that are secondary to amputation are reported in 13-40% of cases and are one of the most challenging types of lower extremity wounds to heal. These patients often have compromised healing capacity. Kayssi et al studied Canadian readmission rates, early (<30 days) and late (30-365) readmissions were attributed to stump complications in 13% and 10% of patients respectively. Wound complications in major limb amputation frequently result in the need for further major surgery in a group of patients with significant co-morbidity and enhanced operative risk. 1, 3, and 5 year reamputation rates for diabetics who have had major amputations are 4.7%, 11.8%, and 13.3% respectively. Henry et al suggested that undergoing multiple amputation revisions may indicate aggressive measures to treat critical limb ischemia or chronic infection that precede conversion to a more proximal amputation. Kono et al studied the incidence and risk factors for reamputation after forefoot amputation. They found that 16/116 (14%) patients developed postoperative infection, and 10 of these required reamputation (62.5%). Five of the ten reamputations occurred within 30 days after the patients developed postoperative infections. In addition to the morbidity from infection there is also an increased rate of phantom pain as well as a delay to mobilisation with prosthesis. Minimizing postoperative infections would likely have improvements in clinical outcomes, quality of life, and utilization of resources. Currently, all patients are given prophylactic broad spectrum antibiotics to reduce the incidence of wound infection. Sadat et al investigated whether a prolonged 5 day course of antibiotics wound reduce stump infections, their results were positive however this treatment is associated with the increased risk of antimicrobial resistance and c. difficile infection. Negative-pressure wound therapy (NPWT) has traditionally been used for the treatment of open wounds. In recent years, the indication for NPWT has been extended to include treatment of closed surgical incisions. Armstrong et al conducted a randomized controlled trial to determine whether NPWT delivered by the VAC system was clinically efficacious in treating amputation wounds of the diabetic foot to improve the proportion of wounds with complete closure. Treatment with NPWT resulted in a higher proportion of wounds that healed, faster healing rates, and fewer re-amputations than with standard treatment. No randomized controlled trials have been performed to assess NPWT and infection rates after major lower limb amputation. There is a paucity of scientific literature reporting outcomes following major amputation in patients with critical limb ischemia, particularly with regards to wound problems and infection. The purpose of this study is to provide Level I evidence on whether negative pressure wound therapy is an effective strategy to significantly reduce postoperative infections after major lower extremity amputation, thereby reducing patient morbidity and mortality from this procedure.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Amputation Wound, Amputation Stump Complication, Amputation Stump; Infection, Infection

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    290 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Negative pressure wound therapy
    Arm Type
    Experimental
    Arm Description
    A vacuum assisted closure device will be applied in this arm
    Arm Title
    Standard dressing
    Arm Type
    Other
    Arm Description
    Standard dressing will be applied to this arm
    Intervention Type
    Device
    Intervention Name(s)
    Negative pressure wound therapy
    Intervention Description
    Negative pressure wound therapy is a commonly utilized tool in the hospital setting and will be applied to amputations in our study to determine the effect on surgical site infections
    Intervention Type
    Other
    Intervention Name(s)
    Standard dressing
    Intervention Description
    A standard dressing will be applied to the amputations in this arm of the study
    Primary Outcome Measure Information:
    Title
    Surgical site infection
    Description
    Surgical site infection will be defined using the Centre for Disease Control and Prevention Guidelines.
    Time Frame
    30 days
    Secondary Outcome Measure Information:
    Title
    Length of stay
    Description
    length of hospital stay
    Time Frame
    30 days
    Title
    Antibiotic use
    Description
    requirement for antibiotics to treat surgical site infection
    Time Frame
    30 days
    Title
    Reoperation
    Description
    requirement for revision of amputation
    Time Frame
    30 days
    Title
    Death
    Description
    mortality
    Time Frame
    30 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: any patient 18 years or older undergoing amputation of the lower limb, either an above knee amputation (AKA) or below knee amputation (BKA) ability to read and write English to undergo informed consent Exclusion Criteria: patients in which a complete seal cannot be obtained at the time of vacuum placement wounds that are not closed primarily existing infection patient is anticipated to not follow-up inability to read and write English
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Oonagh Scallan, MD
    Phone
    6478761954
    Email
    oonagh.scallan@lhsc.on.ca
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Adam Power, MD
    Organizational Affiliation
    London Health Sciences Centre
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

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    RCT on NPWT for Incisions Following Major Lower-limb Amputation to Reduce Surgical Site Infection

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