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Ewing Amputation in Veterans With PAD Undergoing BKA

Primary Purpose

Peripheral Arterial Disease

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Ewing Amputation
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Peripheral Arterial Disease focused on measuring amputation

Eligibility Criteria

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

Inclusion Criteria:

  • Veterans who have reasonable blood flow to heal a TTA (defined as palpable popliteal pulse or palpable femoral pulse with popliteal artery signal)
  • Veterans with an expectation of participating in rehabilitation and resuming ambulation after amputation (defined by the Veteran interest, recent ambulation by the Veteran, ability to participate in physical therapy as deemed by the investigators' physical therapy team)
  • Veterans who will be undergoing below knee amputation for reasons other than infection (uninfected patients) or Veterans who have had foot infection localized below the ankle (retinaculum uninfected) that has been adequately debrided and treated with appropriate antibiotic course.

Exclusion Criteria:

  • Veterans with end-stage renal disease (ESRD)
  • Veterans requiring major amputation due to infection that includes the ankle retinaculum
  • Veterans deemed to have inadequate blood flow to heal a TTA
  • Veterans who cannot participate in rehabilitation or are not expected to be able to ambulate with a prosthesis for any reason;

Sites / Locations

  • Atlanta VA Medical and Rehab Center, Decatur, GARecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Ewing Amputation

Arm Description

Single Arm Pilot Study : To implement lead-in surgeon training and test the feasibility of recruiting and retention of veterans undergoing Ewing Amputation in a single arm study at Atlanta VAMC.

Outcomes

Primary Outcome Measures

PROMIS Numeric Rating Scale
Patient reported rating scale to assess pain intensity and pain interference.
Socket Comfort Score
Patient reported rating scale to assess socket fit of prosthesis.
Phantom and Residual Limb Questionnaire
Patient reported questionnaire to assess sensation in phantom limb.
Lower Extremity Amputee Data Collection Form
Patient reported questionnaire to assess amputation system of care.
Lower Limb Mobility Rating Scale
Patient reported scale to assess movement with prosthetic leg.
Amputee Single Item Mobility Measure
Patient reported measure to assess current level of mobility.
Activities-specific Balance Scale
Patient reported scale to assess balance while performing every day activities.
Self-Reported Falls Measure
Patient reported one question survey to calculate falls in the previous month.
RAND Health Survey
Patient reported survey to assess general health while performing usual activities.
CRIS Fixed Form Instrument
Patient reported rating scale to assess usual activities in previous two weeks.
Patient Two Minute Walk Test
To measure distance patient can walk without assistance in 2 minutes.
Patient Timed Up and Go Test
To measure amount of time patient walks 3 meters.
Berg Balance Scale
To assess the patient's sitting and standing balance levels.
Amputee Mobility Predictor Questionnaire
To measure the patient's sitting, standing, turning and walking/stepping with and without prosthesis.

Secondary Outcome Measures

Full Information

First Posted
June 14, 2022
Last Updated
October 4, 2023
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT05437562
Brief Title
Ewing Amputation in Veterans With PAD Undergoing BKA
Official Title
Pilot Investigation of Ewing Amputation in Veterans With Peripheral Arterial Disease Undergoing Below Knee Amputation
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 1, 2022 (Actual)
Primary Completion Date
September 30, 2024 (Anticipated)
Study Completion Date
September 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development

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
Yes

5. Study Description

Brief Summary
The objective is to quantify in 2 years the feasibility of recruiting and retaining Veterans at the AVAMC in an EA protocol. The investigators will implement a training protocol for AMI and RPNI. The investigators will document competence and timing to competence for the AVAHCS surgical team. The investigators will perform EA in AVAHCS Veterans who meet inclusion/exclusion parameters and elect EA surgical intervention. Veterans will then participate in the investigators' postoperative protocol out to 6 months. The criteria to moving to phase 2 includes clinically consenting and and performing EA in 30 Veterans and collecting 6 months follow up data over 18 months at AVAHCS and 70% or better complete follow-up at 6 month time point after operation.
Detailed Description
Major amputations lead to significant challenges for Veterans and their loved ones. Thus, amputations and the care of amputees are a major focus of the VHA. Hence, the tripartite goals of the VHA Amputation System of Care (ASoC) are to: provide state of the art care, maximize health and independence, and to be the provider of choice for amputated Veterans. Veterans undergo ~1000 transtibial amputations (TTA) annually, making TTA a commonly performed operation in the VA. Almost all Veterans requiring TTA are dysvascular with peripheral artery disease (PAD) and/or diabetes. TTA is a safe operation with a low 30-day mortality rate, and ambulation with prosthesis rates are much better for TTA versus transfemoral amputations (TFA). Since ~50% of Veterans are satisfied with their ambulation after major amputation, improving ambulation is an important benchmark forward in the care of Veterans. Importantly, the lower ambulation rates in Veterans are attributed to modifiable sequelae of major amputation, including: slower wound healing9,10; chronic pain, imbalance, and falls. Excitingly, new techniques can improve pain and balance and may improve wound healing/prevent falls. Ewing amputation (EA) recreates the agonist-antagonist myoneural interface (AMI) maintaining muscle tension, proprioception and limiting fibrofatty muscle degeneration of muscle flaps. EA also creates regenerative peripheral neural interfaces (RPNI) to improve pain control. Thus, EA may have a significant benefit to Veterans undergoing TTA.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Arterial Disease
Keywords
amputation

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Collect feasibility criteria for recruitment, retention, and data collection.
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ewing Amputation
Arm Type
Other
Arm Description
Single Arm Pilot Study : To implement lead-in surgeon training and test the feasibility of recruiting and retention of veterans undergoing Ewing Amputation in a single arm study at Atlanta VAMC.
Intervention Type
Other
Intervention Name(s)
Ewing Amputation
Intervention Description
All patients will receive Ewing Amputation to test feasibility.
Primary Outcome Measure Information:
Title
PROMIS Numeric Rating Scale
Description
Patient reported rating scale to assess pain intensity and pain interference.
Time Frame
12 months
Title
Socket Comfort Score
Description
Patient reported rating scale to assess socket fit of prosthesis.
Time Frame
12 months
Title
Phantom and Residual Limb Questionnaire
Description
Patient reported questionnaire to assess sensation in phantom limb.
Time Frame
12 months
Title
Lower Extremity Amputee Data Collection Form
Description
Patient reported questionnaire to assess amputation system of care.
Time Frame
12 months
Title
Lower Limb Mobility Rating Scale
Description
Patient reported scale to assess movement with prosthetic leg.
Time Frame
12 months
Title
Amputee Single Item Mobility Measure
Description
Patient reported measure to assess current level of mobility.
Time Frame
12 months
Title
Activities-specific Balance Scale
Description
Patient reported scale to assess balance while performing every day activities.
Time Frame
12 months
Title
Self-Reported Falls Measure
Description
Patient reported one question survey to calculate falls in the previous month.
Time Frame
12 months
Title
RAND Health Survey
Description
Patient reported survey to assess general health while performing usual activities.
Time Frame
12 months
Title
CRIS Fixed Form Instrument
Description
Patient reported rating scale to assess usual activities in previous two weeks.
Time Frame
12 months
Title
Patient Two Minute Walk Test
Description
To measure distance patient can walk without assistance in 2 minutes.
Time Frame
12 months
Title
Patient Timed Up and Go Test
Description
To measure amount of time patient walks 3 meters.
Time Frame
12 months
Title
Berg Balance Scale
Description
To assess the patient's sitting and standing balance levels.
Time Frame
12 months
Title
Amputee Mobility Predictor Questionnaire
Description
To measure the patient's sitting, standing, turning and walking/stepping with and without prosthesis.
Time Frame
12 months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Veterans who have reasonable blood flow to heal a TTA (defined as palpable popliteal pulse or palpable femoral pulse with popliteal artery signal) Veterans with an expectation of participating in rehabilitation and resuming ambulation after amputation (defined by the Veteran interest, recent ambulation by the Veteran, ability to participate in physical therapy as deemed by the investigators' physical therapy team) Veterans who will be undergoing below knee amputation for reasons other than infection (uninfected patients) or Veterans who have had foot infection localized below the ankle (retinaculum uninfected) that has been adequately debrided and treated with appropriate antibiotic course. Exclusion Criteria: Veterans with end-stage renal disease (ESRD) Veterans requiring major amputation due to infection that includes the ankle retinaculum Veterans deemed to have inadequate blood flow to heal a TTA Veterans who cannot participate in rehabilitation or are not expected to be able to ambulate with a prosthesis for any reason;
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Luke P Brewster, MD
Phone
(404) 321-6111
Ext
7084
Email
Luke.Brewster@va.gov
First Name & Middle Initial & Last Name or Official Title & Degree
Madhur Sancheti, MS
Phone
(404) 321-6111
Ext
206478
Email
madhur.sancheti@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luke P Brewster, MD
Organizational Affiliation
Atlanta VA Medical and Rehab Center, Decatur, GA
Official's Role
Principal Investigator
Facility Information:
Facility Name
Atlanta VA Medical and Rehab Center, Decatur, GA
City
Decatur
State/Province
Georgia
ZIP/Postal Code
30033-4004
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Luke P Brewster, MD
Phone
404-321-6111
Ext
7084
Email
Luke.Brewster@va.gov
First Name & Middle Initial & Last Name & Degree
Ashley N Scales
Phone
(404) 321-6111
Ext
23952
Email
Ashley.Scales@va.gov
First Name & Middle Initial & Last Name & Degree
Luke P Brewster, MD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Ewing Amputation in Veterans With PAD Undergoing BKA

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