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Sutures Versus Staples for Wound Closure in Orthopaedic Surgery

Primary Purpose

Surgical Wound Infection

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Sutures
Staples
Sponsored by
University of Manitoba
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Surgical Wound Infection focused on measuring Surgical, Infection, Post-operative, Sutures, Staples

Eligibility Criteria

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

Inclusion Criteria:

  • Adult patients (>18 years old)
  • All open orthopedic procedures
  • Largest wound >2cm in length

Exclusion Criteria:

  • Open fracture
  • Known nickel allergy
  • Active infection (any site)
  • Chemotherapy during study period (1 month prior until end of follow-up)
  • Radiation therapy to surgical site (1 month prior until end of follow-up)
  • Foot surgery (any site)
  • Hand surgery (including carpal surgery)
  • Arthroscopic procedures

Sites / Locations

  • Concordia Hip and Knee Institute
  • Health Sciences Centre
  • Pan Am Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Sutures

Staples

Arm Description

Orthopedic surgical wound closed with sutures

Orthopedic surgical wound closed with metallic staples

Outcomes

Primary Outcome Measures

Surgical site infection
Suspected cases will be identified by one or all of the following: use of intravenous antibiotics, use of oral antibiotics (patient self-reported), re-operation at same site. A blinded committee will adjudicate each suspected case and determine true infections using available clinical information. Agreement will be determined by vote.

Secondary Outcome Measures

Additional healthcare contact related to their surgery
As defined by self-reported visits to other healthcare professionals.
Dressing changes by homecare/patient at home
Defined by homecare consult records and patient self-report
Length of stay
Based on admission and discharge dates
Wound drainage
As defined by necessity for dressing changes after 72 hours for fluid leakage
Wound necrosis
Evidence of marginal skin death at the surgical site as evidenced by skin slough, blackening or liquefaction
Patient satisfaction with wound appearance
Using visual analogue scale
Visual analogue pain score for suture/staple removal
Patients will rate the pain experienced in removing the wound closure materials in clinic prior to unblinding.

Full Information

First Posted
June 14, 2010
Last Updated
October 12, 2018
Sponsor
University of Manitoba
Collaborators
Manitoba Medical Service Foundation, Gibson Orthopaedic Fund for Research and Education
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1. Study Identification

Unique Protocol Identification Number
NCT01146236
Brief Title
Sutures Versus Staples for Wound Closure in Orthopaedic Surgery
Official Title
Sutures vs Staples for Wound Closure in Orthopaedic Surgery: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
July 2010 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Manitoba
Collaborators
Manitoba Medical Service Foundation, Gibson Orthopaedic Fund for Research and Education

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The trial is a randomized, controlled trial. Adult patients undergoing orthopaedic surgical procedures would be randomized to one of two groups for surgical wound closure, skin sutures or skin staples. The primary outcome measures would be surgical site infection indicated by the use of oral or intravenous antibiotics for suspected wound infection and/or re-operation at the same site. Patients would be followed up as per their usual post-operative course for a total of three months in the trauma and spine population and six months in the total joint arthroplasty population. It is hypothesized that wounds closed with sutures and staples will have similar infection rates as defined by the use of antibiotics or reoperation.
Detailed Description
To date, there is no clear consensus on the method that is best for closure of surgical wounds in orthopaedic surgery. Orthopaedic surgeons have a multitude of wound closure habits. A recent meta-analysis comparing staples to sutures in wound closure demonstrated a three-fold increase in infection in stapled wounds compared to sutured wounds. The studies used in the meta-analysis were primarily of poor methodological quality. A large, well-designed randomized, controlled trial is needed to guide orthopedic surgeons in their choice of wound closure materials. This study would attempt to provide information on the use of sutures versus skin staples and the effect on the development of surgical site infections in adults undergoing orthopaedic procedures. A parallel group randomized controlled trial with institutional review board approval will be conducted. Patients will be randomized intraoperatively to have skin wounds closed with sutures or staples. Dressings will be used to maintain blinding of participants and outcome assessors. The primary outcome measure will be infections adjudicated by a blinded data safety monitoring committee. Suspected infections will be defined by: Use of antibiotics or reoperation for infection at the operative site within three months (six months for arthroplasty subgroup) The independent review, board blinded to treatment assignment, will adjudicate suspected infections based on clinical data. A cost analysis will also be performed to compare the costs associated with wounds closed with sutures and staples from a health care institution perspective. All data will be analyzed by a blinded epidemiologist. Dichotomous primary and secondary outcome measures will be analyzed using the Chi-squared statistic. Continuous outcome measures will be analyzed using Student's t-test. Subgroup analysis will compare infection rates using sutures versus staples in each anatomic area (upper extremity, pelvis/acetabulum, hip/femur, knee, ankle). A further subgroup analysis will be conducted comparing trauma patients to elective patients. Non-infected revision surgery will also be compared to primary surgery. It is hypothesized that wounds closed with sutures and staples will have similar infection rates as defined by the use of antibiotics or reoperation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Surgical Wound Infection
Keywords
Surgical, Infection, Post-operative, Sutures, Staples

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
247 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sutures
Arm Type
Active Comparator
Arm Description
Orthopedic surgical wound closed with sutures
Arm Title
Staples
Arm Type
Active Comparator
Arm Description
Orthopedic surgical wound closed with metallic staples
Intervention Type
Device
Intervention Name(s)
Sutures
Intervention Description
Orthopedic surgical wounds closed with sutures
Intervention Type
Device
Intervention Name(s)
Staples
Intervention Description
Orthopedic surgical wounds closed with metallic staples
Primary Outcome Measure Information:
Title
Surgical site infection
Description
Suspected cases will be identified by one or all of the following: use of intravenous antibiotics, use of oral antibiotics (patient self-reported), re-operation at same site. A blinded committee will adjudicate each suspected case and determine true infections using available clinical information. Agreement will be determined by vote.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Additional healthcare contact related to their surgery
Description
As defined by self-reported visits to other healthcare professionals.
Time Frame
6 months
Title
Dressing changes by homecare/patient at home
Description
Defined by homecare consult records and patient self-report
Time Frame
6 months
Title
Length of stay
Description
Based on admission and discharge dates
Time Frame
6 months
Title
Wound drainage
Description
As defined by necessity for dressing changes after 72 hours for fluid leakage
Time Frame
6 months
Title
Wound necrosis
Description
Evidence of marginal skin death at the surgical site as evidenced by skin slough, blackening or liquefaction
Time Frame
6 months
Title
Patient satisfaction with wound appearance
Description
Using visual analogue scale
Time Frame
6 months
Title
Visual analogue pain score for suture/staple removal
Description
Patients will rate the pain experienced in removing the wound closure materials in clinic prior to unblinding.
Time Frame
2 weeks post-operative

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients (>18 years old) All open orthopedic procedures Largest wound >2cm in length Exclusion Criteria: Open fracture Known nickel allergy Active infection (any site) Chemotherapy during study period (1 month prior until end of follow-up) Radiation therapy to surgical site (1 month prior until end of follow-up) Foot surgery (any site) Hand surgery (including carpal surgery) Arthroscopic procedures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jesse Shantz, MD, MBA
Organizational Affiliation
University of Manitoba
Official's Role
Principal Investigator
Facility Information:
Facility Name
Concordia Hip and Knee Institute
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R2K 2M9
Country
Canada
Facility Name
Health Sciences Centre
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R3A 1R9
Country
Canada
Facility Name
Pan Am Clinic
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R3M 3E4
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
23394586
Citation
Slade Shantz JA, Vernon J, Morshed S, Leiter J, Stranges G. Sutures versus staples for wound closure in orthopaedic surgery: a pilot randomized controlled trial. Patient Saf Surg. 2013 Feb 9;7(1):6. doi: 10.1186/1754-9493-7-6.
Results Reference
derived
PubMed Identifier
22672186
Citation
Shantz JA, Vernon J, Leiter J, Morshed S, Stranges G. Sutures versus staples for wound closure in orthopaedic surgery: a randomized controlled trial. BMC Musculoskelet Disord. 2012 Jun 6;13:89. doi: 10.1186/1471-2474-13-89.
Results Reference
derived

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Sutures Versus Staples for Wound Closure in Orthopaedic Surgery

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