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Fluid Lavage of Open Wounds (FLOW): Pilot Trial (FLOW)

Primary Purpose

Infection, Wound Healing Problem, Nonunion

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Type of fluid lavage solution
Type of fluid lavage pressure
Sponsored by
McMaster University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infection focused on measuring open wound, solution, pressure, randomized

Eligibility Criteria

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

Inclusion Criteria:

  • skeletally mature
  • sustained an open fracture of the appendicular skeleton (type I to IIIb).

Exclusion Criteria:

  • vascular deficit
  • [any] allergy to detergents or castile soap
  • previous wound infection or osteomyelitis
  • previous fracture with retained hardware in the injured extremity
  • operative management more than 24 hours after injury
  • use of immunosuppressive medication within six months
  • immunological deficiency or disease conditions
  • fractures of the hands (distal to the carpus) or toes

Sites / Locations

  • University of Missouri Health Care
  • Greenville Hospital System
  • East Texas Medical Centre
  • Queen Elizabeth II Health Sciences Centre
  • Hamilton Health Sciences
  • Ottawa Hospital - Civic Campus
  • St. Michael's Hospital
  • Sunnybrook Health Sciences Centre
  • Sancheti Institute for Orthopaedics & Rehabilitation

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Normal saline and High pressure

Soap solution and High pressure

Normal saline and Low pressure

Soap solution and Low pressure

Arm Description

Irrigation with normal saline delivered at high pressure

Irrigation with soap solution delivered at high pressure

Irrigation with saline solution delivered at low pressure

Irrigation with soap solution delivered at low pressure

Outcomes

Primary Outcome Measures

The Number of Participants With Re-operations (All Subsequent Operative Procedures to Treat an Infection, a Wound Healing Problem, or a Nonunion).

Secondary Outcome Measures

The Number of Participants With All Operative and Non-operatively Managed Infections, Wound Healing Problems, and Nonunions.
Mean Difference in Health-related Quality of Life and Physical Function From Baseline (Pre-injury) to 12 Months Measured by the SF-12 Questionnaire (Solution).
Solution and pressure were analyzed separately for this outcome. The SF-12 summary scores (PCS-12 and MCS-12) ranges from 0 to 100. Higher scores indicate that a person has better health status, while lower scores indicate poorer health status. Please note that the values reported are mean differences in scores from baseline (pre-injury) to 12 months per arm.
Mean Difference in Health-related Quality of Life and Physical Function From Baseline (Pre-injury) to 12 Months Measured by the EQ-5D Questionnaire (Solution).
Solution and pressure were analyzed separately for this outcome. The EQ-5D summary score ranges from 0 to 1. Higher scores indicate that a person has a better health-related quality of life, while lower scores indicate worse health-related quality of life. Please note that the values reported are mean differences in scores from baseline (pre-injury) to 12 months per arm.
Mean Difference in Health-related Quality of Life and Physical Function From Baseline (Pre-injury) to 12 Months Measured by the SF-12 Questionnaire (Pressure)
Solution and pressure were analyzed separately for this outcome. The SF-12 summary scores (PCS-12 and MCS-12) ranges from 0 to 100. Higher scores indicate that a person has better health status, while lower scores indicate poorer health status. Please note that the values reported are mean differences in scores from baseline (pre-injury) to 12 months per arm.
Mean Difference in Health-related Quality of Life and Physical Function From Baseline (Pre-injury) to 12 Months Measured by the EQ-5D Questionnaire (Pressure)
Solution and pressure were analyzed separately for this outcome. The EQ-5D summary score ranges from 0 to 1. Higher scores indicate that a person has a better health-related quality of life, while lower scores indicate worse health-related quality of life. Please note that the values reported are mean differences in scores from baseline (pre-injury) to 12 months.

Full Information

First Posted
February 16, 2010
Last Updated
March 15, 2019
Sponsor
McMaster University
Collaborators
The Physicians' Services Incorporated Foundation, Orthopaedic Trauma Association
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1. Study Identification

Unique Protocol Identification Number
NCT01069315
Brief Title
Fluid Lavage of Open Wounds (FLOW): Pilot Trial
Acronym
FLOW
Official Title
Fluid Lavage of Open Wounds (FLOW): A Multi-Center, Blinded, Factorial Pilot Trial Comparing Alternative Irrigating Solutions and Pressures in Patients With Open Fractures
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
July 2006 (undefined)
Primary Completion Date
June 2008 (Actual)
Study Completion Date
June 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
McMaster University
Collaborators
The Physicians' Services Incorporated Foundation, Orthopaedic Trauma Association

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this trial is to investigate whether irrigation solution (soap vs. saline solution), or irrigation pressure (high vs. low) will decrease the rate of infection among patients with open fracture wounds.
Detailed Description
Open fractures are an important source of morbidity and are associated with delayed union, nonunion, and infection. Preventing infection through meticulous irrigation and debridement is an important goal in management, and different lavage fluids and irrigation techniques (e.g. high or low pressure lavage) have been described for this purpose. There are, however, a limited number of randomized trials comparing irrigating solutions or irrigating technique. We compared the use of castile soap versus normal saline, as well as high versus low pressure pulsatile lavage on the rates of reoperations and complications in patients with open fracture wounds.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infection, Wound Healing Problem, Nonunion
Keywords
open wound, solution, pressure, randomized

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
111 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Normal saline and High pressure
Arm Type
Experimental
Arm Description
Irrigation with normal saline delivered at high pressure
Arm Title
Soap solution and High pressure
Arm Type
Experimental
Arm Description
Irrigation with soap solution delivered at high pressure
Arm Title
Normal saline and Low pressure
Arm Type
Experimental
Arm Description
Irrigation with saline solution delivered at low pressure
Arm Title
Soap solution and Low pressure
Arm Type
Experimental
Arm Description
Irrigation with soap solution delivered at low pressure
Intervention Type
Procedure
Intervention Name(s)
Type of fluid lavage solution
Intervention Description
Comparison of castile soap solution vs. normal saline solution.
Intervention Type
Procedure
Intervention Name(s)
Type of fluid lavage pressure
Intervention Description
Comparison of low pressure vs. high pressure.
Primary Outcome Measure Information:
Title
The Number of Participants With Re-operations (All Subsequent Operative Procedures to Treat an Infection, a Wound Healing Problem, or a Nonunion).
Time Frame
one year
Secondary Outcome Measure Information:
Title
The Number of Participants With All Operative and Non-operatively Managed Infections, Wound Healing Problems, and Nonunions.
Time Frame
1 year
Title
Mean Difference in Health-related Quality of Life and Physical Function From Baseline (Pre-injury) to 12 Months Measured by the SF-12 Questionnaire (Solution).
Description
Solution and pressure were analyzed separately for this outcome. The SF-12 summary scores (PCS-12 and MCS-12) ranges from 0 to 100. Higher scores indicate that a person has better health status, while lower scores indicate poorer health status. Please note that the values reported are mean differences in scores from baseline (pre-injury) to 12 months per arm.
Time Frame
1 year
Title
Mean Difference in Health-related Quality of Life and Physical Function From Baseline (Pre-injury) to 12 Months Measured by the EQ-5D Questionnaire (Solution).
Description
Solution and pressure were analyzed separately for this outcome. The EQ-5D summary score ranges from 0 to 1. Higher scores indicate that a person has a better health-related quality of life, while lower scores indicate worse health-related quality of life. Please note that the values reported are mean differences in scores from baseline (pre-injury) to 12 months per arm.
Time Frame
one year
Title
Mean Difference in Health-related Quality of Life and Physical Function From Baseline (Pre-injury) to 12 Months Measured by the SF-12 Questionnaire (Pressure)
Description
Solution and pressure were analyzed separately for this outcome. The SF-12 summary scores (PCS-12 and MCS-12) ranges from 0 to 100. Higher scores indicate that a person has better health status, while lower scores indicate poorer health status. Please note that the values reported are mean differences in scores from baseline (pre-injury) to 12 months per arm.
Time Frame
one year
Title
Mean Difference in Health-related Quality of Life and Physical Function From Baseline (Pre-injury) to 12 Months Measured by the EQ-5D Questionnaire (Pressure)
Description
Solution and pressure were analyzed separately for this outcome. The EQ-5D summary score ranges from 0 to 1. Higher scores indicate that a person has a better health-related quality of life, while lower scores indicate worse health-related quality of life. Please note that the values reported are mean differences in scores from baseline (pre-injury) to 12 months.
Time Frame
one year

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: skeletally mature sustained an open fracture of the appendicular skeleton (type I to IIIb). Exclusion Criteria: vascular deficit [any] allergy to detergents or castile soap previous wound infection or osteomyelitis previous fracture with retained hardware in the injured extremity operative management more than 24 hours after injury use of immunosuppressive medication within six months immunological deficiency or disease conditions fractures of the hands (distal to the carpus) or toes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohit Bhandari, MD, FRCSC
Organizational Affiliation
McMaster University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Mohit Bhandari, MD, FRCSC
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Gordon Guyatt, MD, FRCSC
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kyle J Jeray, MD, FRCSC
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Missouri Health Care
City
Columbia
State/Province
Missouri
Country
United States
Facility Name
Greenville Hospital System
City
Greenville
State/Province
South Carolina
Country
United States
Facility Name
East Texas Medical Centre
City
Tyler
State/Province
Texas
Country
United States
Facility Name
Queen Elizabeth II Health Sciences Centre
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
B3H 2A7
Country
Canada
Facility Name
Hamilton Health Sciences
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8L 8E7
Country
Canada
Facility Name
Ottawa Hospital - Civic Campus
City
Ottawa
State/Province
Ontario
Country
Canada
Facility Name
St. Michael's Hospital
City
Toronto
State/Province
Ontario
Country
Canada
Facility Name
Sunnybrook Health Sciences Centre
City
Toronto
State/Province
Ontario
Country
Canada
Facility Name
Sancheti Institute for Orthopaedics & Rehabilitation
City
Pune
State/Province
Maharashtra
Country
India

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
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derived

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Fluid Lavage of Open Wounds (FLOW): Pilot Trial

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