Study to Determine if Different Prosthetic Sockets Effect How Much Oxygen is in the Tissue of Lower Limb Amputees While They Are Walking
Primary Purpose
Amputation, Diabetes Complications, Leg Injuries
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pe-Lite and sleeve suspension socket
Total Surface bearing a socket with a sleeve suspension but without suction
Total surface bearing suction socket with a pin lock suspension
Total surface bearing suction socket with a sleeve suspension
Vacuum-assisted socket system (Harmony System, Otto Bock)
Sponsored by
About this trial
This is an interventional treatment trial for Amputation focused on measuring Artificial limbs, Gait, Oximetry, Prosthesis, Rehabilitation
Eligibility Criteria
Inclusion Criteria:
All subjects must meet the following inclusion criteria:
- unilateral transtibial amputee of diabetic etiology between the ages of 18 and 70,
- have been fit with a prosthesis and have used a prosthesis for at least one year,
- wear the prosthesis at least 4 hours per day,
- ambulate without upper extremity aids, and
- have no history of injurious falls within the previous six months.
Exclusion Criteria:
Subjects will be excluded if:
- they have a significant lower extremity pain condition, musculoskeletal disorder, or neurological deficit that interferes with their ability to pursue typical daily activities or alters their gait characteristics or
- their residual limb is ulcerated.
Sites / Locations
- VA Puget Sound Health Care System Seattle Division, Seattle, WA
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Arm 1
Arm Description
Comparison of five different clinically used suspension and socket systems
Outcomes
Primary Outcome Measures
Oxygen in tissue
Tissue oxygen saturation (StO2)
Secondary Outcome Measures
Full Information
NCT ID
NCT00985842
First Posted
December 11, 2007
Last Updated
June 28, 2018
Sponsor
VA Office of Research and Development
Collaborators
University of Washington
1. Study Identification
Unique Protocol Identification Number
NCT00985842
Brief Title
Study to Determine if Different Prosthetic Sockets Effect How Much Oxygen is in the Tissue of Lower Limb Amputees While They Are Walking
Official Title
Socket System Effect on Tissue Oxygenation During Amputee Gait
Study Type
Interventional
2. Study Status
Record Verification Date
June 2018
Overall Recruitment Status
Completed
Study Start Date
November 1, 2009 (Actual)
Primary Completion Date
October 26, 2012 (Actual)
Study Completion Date
October 26, 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development
Collaborators
University of Washington
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Amputee gait produces periodic occlusion of residual limb blood vessels. During the stance phase of gait, body weight cause the prosthesis to compresses the soft tissue of the residual limb and occlude blood flow. This occlusion can be relieved during swing phase, but may depend on type of prosthesis. The purpose of the proposed research is to: (1) discover the range of tissue oxygenation in the intact and residual lower limbs of dysvascular amputees during gait and (2) to learn which of five different prosthetic limb systems provides greater tissue oxygenation.
Detailed Description
The amount of oxygen in residual limb tissue is an important health status indicator; resistance to infection, promotion of wound healing, production of collagen, and epithelialization all correlate with higher oxygen levels. Unfortunately, simply donning a lower limb prosthesis may limit circulation and reduce the level of tissue oxygenation. This reduction may be compounded by the biomechanical forces of gait. The compressive loads of the body's weight during stance and the inertial loads of the prosthesis during swing may further occlude circulation, albeit by different mechanisms.
For the dysvascular lower limb amputee, the choice of prosthetic socket and suspension system may impact the overall health of their residual limb and wound healing capacity. An inappropriate choice may lead to skin irritation, tissue breakdown, discomfort, and reduced mobility. For these patients, any component that reduces tissue oxygenation is a significant problem because compromised circulation can forestall wound healing.
The objective of the proposed research is to use photo-oximetry to discover which of five different prosthetic limb systems results in higher residual limb tissue oxygenation during both rest and gait. This experiment will enable evidence-based decision making on this clinically relevant problem. Using a prospective, randomized cross-over experimental design and the investigators' photo-oximetry system, the investigators will measure and compare the tissue oxygenation along the medial and lateral surfaces (3 sites each) of the residual limb during rest and walking.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Amputation, Diabetes Complications, Leg Injuries, Traumatic Amputation
Keywords
Artificial limbs, Gait, Oximetry, Prosthesis, Rehabilitation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
7 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Arm 1
Arm Type
Other
Arm Description
Comparison of five different clinically used suspension and socket systems
Intervention Type
Device
Intervention Name(s)
Pe-Lite and sleeve suspension socket
Intervention Description
Prosthetic socket worn by the amputee that has a Pe-lite foam liner between the socket and the residual limb. It is suspended from the residual limb using a sleeve at the top of the socket.
Intervention Type
Device
Intervention Name(s)
Total Surface bearing a socket with a sleeve suspension but without suction
Intervention Description
Prosthetic socket worn by the amputee where the fit of the socket touches every part of the residual limb. This socket is suspended from the residual limb using a sleeve at the top of the socket.
Intervention Type
Device
Intervention Name(s)
Total surface bearing suction socket with a pin lock suspension
Intervention Description
Prosthetic socket worn by the amputee where the fit of the socket touches every part of the residual limb. This socket is suspended from the residual limb using a pin that protrudes from the bottom of the liner into the socket that is then locked in place by the amputee.
Intervention Type
Device
Intervention Name(s)
Total surface bearing suction socket with a sleeve suspension
Intervention Description
Prosthetic socket worn by the amputee where the fit of the socket touches every part of the residual limb. This socket using vacuum suction plus a sleeve at the top of the prosthetic socket to enhance the security of the suspension.
Intervention Type
Device
Intervention Name(s)
Vacuum-assisted socket system (Harmony System, Otto Bock)
Intervention Description
Prosthetic socket worn by the amputee where the a vacuum pump, in this case a mechanically-activated pump, creates a vacuum between the socket and the limb. This vacuum suspends the prosthetic limb from the amputee's residual limb.
Primary Outcome Measure Information:
Title
Oxygen in tissue
Description
Tissue oxygen saturation (StO2)
Time Frame
Comparison of five different systems will be performed in one session occurring on one day
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All subjects must meet the following inclusion criteria:
unilateral transtibial amputee of diabetic etiology between the ages of 18 and 70,
have been fit with a prosthesis and have used a prosthesis for at least one year,
wear the prosthesis at least 4 hours per day,
ambulate without upper extremity aids, and
have no history of injurious falls within the previous six months.
Exclusion Criteria:
Subjects will be excluded if:
they have a significant lower extremity pain condition, musculoskeletal disorder, or neurological deficit that interferes with their ability to pursue typical daily activities or alters their gait characteristics or
their residual limb is ulcerated.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Glenn K Klute, PhD
Organizational Affiliation
VA Puget Sound Health Care System Seattle Division, Seattle, WA
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Puget Sound Health Care System Seattle Division, Seattle, WA
City
Seattle
State/Province
Washington
ZIP/Postal Code
98108
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Links:
URL
http://www.amputation.research.va.gov/
Description
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Study to Determine if Different Prosthetic Sockets Effect How Much Oxygen is in the Tissue of Lower Limb Amputees While They Are Walking
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