Purpose

This study will involve the development of a novel approach to lower extremity residual limb surgical revision that offers the promise of augmenting volitional motor control, restore proprioception and reverse atrophy

Condition

Eligibility

Eligible Ages
Between 18 Years and 65 Years
Eligible Genders
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Between the ages of 18-65 - Has already undergone a standard AKA or BKA procedure - Suffers from symptoms such as: - Intractable pain - Deterioration of skin on or around stump - Suffering from other sources of discomfort arising from stump - Intact inherent wound healing - Adequate communication skills - High motivation

Exclusion Criteria

  • Inadequate health to undergo operative procedure using standard anesthesia (i.e. cardiopulmonary) - Individuals with impaired wound healing - Individuals suffering from extensive peripheral neuropathies - Active smokers - Individuals with a history of poor compliance - Women who are pregnant or plan to become pregnant before surgical intervention

Study Design

Phase
N/A
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Intervention Model Description
Prospective clinical trial in which intervention subjects will serve as their own control
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Intervention
Subjects undergoing the proposed operative intervention. Intervention patients will serve as their own control for all outcome measures
  • Procedure: Residual limb revision
    Surgical procedure involving construction of agonist-antagonist myoneural interfaces (AMIs)

Recruiting Locations

Brigham and Women's Hospital
Boston, Massachusetts 02115
Contact:
Matthew J Carty, MD
617-983-4555
mcarty@partners.org

More Details

Status
Recruiting
Sponsor
Brigham and Women's Hospital

Study Contact

Matthew J Carty, MD
6179834555
mcarty@partners.org

Detailed Description

The hypothesis of this research protocol is that we will be able to modify the residual limbs of patients who have already undergone lower extremity amputations so as to include biological actuators that will enable the successful employment of next generation lower extremity prostheses, diminish/eliminate phantom limb pain, restore proprioception and regenerate lost muscle mass. The specific aims of the project are as follows: 1. To develop a standardized operative technique for both above knee (AK) and below knee (BK) amputation revision procedures that includes AMIs to restore musculotendinous proprioceptive capabilities 2. To assess the capacity for these actuators to provide enhanced motor control and sensory feedback, as well as ablate phantom limb symptomatology and augment residual limb muscle mass 3. To determine the reinnervation time course and longevity of these biological constructs 4. To validate the functional and somatosensory superiority of the proposed revision technique over standard approaches to BKA and AKA 5. To develop a modified acute postoperative rehabilitation strategy suited to this new surgical approach

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.