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Randomized Clinical Trial for Ewing Amputation in the VA

Phase 2
Not yet recruiting
Conditions
Peripheral Arterial Disease
Interventions
Other: Ewing Amputation
Registration Number
NCT05437562
Lead Sponsor
VA Office of Research and Development
Brief Summary

This study follows the Pilot Investigation of Ewing Amputation for Veterans with PAD Undergoing a Below Knee Amputation. The 2 year pilot feasibility phase has concluded recruitment and enrollment.

The current phase is a 5 year randomized study of Ewing Below Knee Amputation vs. Standard Below Knee Amputation. If Veterans participate, they will be randomized to either Ewing Amputation or Standard Below Knee Amputation.

The scientific premise motivating this proposal is that Ewing Amputation is a promising surgical technique that may improve walking metrics in dysvascular Veterans by providing a better residual limb and improving pain and balance.

In preparation of this proposal, we have formed multi-disciplinary surgical teams at each site, and we have been supported by a clinical trial planning meeting to garner the considerable expertise in rehabilitation and amputee assessment from VA and DOD experts to assist in the design of this proposal, testing the overall hypothesis that: Ewing Amputation can help Veterans walk.

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.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
120
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
  • Veterans who were randomized for their other limb (to prevent Veteran from the possibility of having 2 different amputations)

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Ewing AmputationEwing AmputationSingle 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.
Primary Outcome Measures
NameTimeMethod
Amputee Single Item Mobility Measure12 months

Patient reported measure to assess current level of mobility.

PROMIS Numeric Rating Scale12 months

Patient reported rating scale to assess pain intensity and pain interference.

Lower Extremity Amputee Data Collection Form12 months

Patient reported questionnaire to assess amputation system of care.

Lower Limb Mobility Rating Scale12 months

Patient reported scale to assess movement with prosthetic leg.

Activities-specific Balance Scale12 months

Patient reported scale to assess balance while performing every day activities.

RAND Health Survey12 months

Patient reported survey to assess general health while performing usual activities.

CRIS Fixed Form Instrument12 months

Patient reported rating scale to assess usual activities in previous two weeks.

Patient Two Minute Walk Test12 months

To measure distance patient can walk without assistance in 2 minutes.

Patient Timed Up and Go Test12 months

To measure amount of time patient walks 3 meters.

Amputee Mobility Predictor Questionnaire12 months

To measure the patient's sitting, standing, turning and walking/stepping with and without prosthesis.

Socket Comfort Score12 months

Patient reported rating scale to assess socket fit of prosthesis.

Phantom and Residual Limb Questionnaire12 months

Patient reported questionnaire to assess sensation in phantom limb.

Self-Reported Falls Measure12 months

Patient reported one question survey to calculate falls in the previous month.

Berg Balance Scale12 months

To assess the patient's sitting and standing balance levels.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (3)

Atlanta VA Medical and Rehab Center, Decatur, GA

🇺🇸

Decatur, Georgia, United States

Tennessee Valley Healthcare System Nashville Campus, Nashville, TN

🇺🇸

Nashville, Tennessee, United States

Michael E. DeBakey VA Medical Center, Houston, TX

🇺🇸

Houston, Texas, United States

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