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View Clinical Trial (Medical Research Study)


Transplantation of Allograft Upper Extremity(Ies) for Treatment of Dominant Hand or Bilateral Amputees

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City:   Boston
State:   Massachusetts
Zip Code:   02115
Conditions:   Upper Extremity Amputation - Hand Amputation
Purpose:   Hand transplantation surgery is the transfer of one or both hands from a deceased human donor to a patient with single dominant hand or bilateral hand amputation. Hand transplantation is an innovative reconstructive procedure that has the potential to significantly improve the lives of hand amputees. The purpose of this study is to develop the best practices for hand transplantation that will improve the outcomes of future hand transplant recipients.
Study Summary:   Hand transplantation surgery, the transfer of the hand(s) from a deceased human donor to a patient with amputation of one or both hands, is an experimental reconstructive procedure that has the potential to significantly improve the lives of hand amputees. Hand transplantation is similar to face transplantation in that the tissues transplanted include skin, tendons, muscles, ligaments, bones and blood vessels. The hand transplant team at Brigham and Women's Hospital includes a wide variety of medical and surgical specialties. The team hopes to build upon the success of their first face transplantation to provide amputee patients with the significant benefits of hand transplantation. Toward this goal, BWH is actively seeking qualified candidates for the hand transplant research study. We will be studying a small group of people to learn more about: - How to advance the science of hand transplantation - How to support and limit transplant rejection issues - How people do after hand transplantation We describe hand transplant surgery as a life-giving procedure because it has the potential to dramatically improve, that is to restore, both a patient's mental and physical health and his/her ability to function and integrate in society. However, as with any other type of organ transplantation, this improvement will require the patient to make a lifetime commitment to taking medications that suppress the body's immune system. Conventional hand reconstruction methods are always considered first, but they may provide less than optimal results for certain patients. There are many sophisticated prostheses that satisfactorily replace the basic function of an upper extremity (upper arm, forearm and hand). However, replacing upper extremities (in whole or in part) with prosthetics remains suboptimal in that prostheses do not provide sensation and do not have a natural appearance. Hand transplant surgery, however, has the potential to deliver these desired functional and aesthetic benefits. Functionally, hand transplant surgery can provide a patient with new hands that, after extensive rehabilitation, allow him/her to perform daily activities and, in most cases, return to work. Furthermore, the ability to restore a near-normal aesthetic appearance of the hand(s) can lead to tremendous psychological benefits, including elevated confidence and mood. From the time we begin our search for a qualified hand transplant recipient to the continuing care we provide following surgery, a significant amount of time, expertise and attentiveness is contributed toward making the procedure a progressive success. Hand transplant candidates go through an extensive screening process that is likely to last several months. This screening includes a psychiatric and social support evaluation and a series of imaging tests to help determine a patient's physical and mental readiness for the procedure. If, upon completion of the screening process, it is determined that a patient is a suitable candidate, we will place the patient on a transplant waiting list. We will then begin working with the New England Organ Bank (NEOB) team to find a donor who matches the recipient's tissue requirements - for example similar age and correct blood type. This search could take many months, and, if a suitable donor is not found within one year, we will speak with the patient to determine whether he/she is willing to continue waiting. When a donor is found, we will immediately inform the patient about when to arrive at the hospital for the operation. As the timing for this type of procedure is extremely important, patients are expected to be readily available, that is, to reside within a 12-hour travel radius of BWH. During the surgery, the parts most likely to be reconstructed include the hand and partial forearm, and in some cases, if necessary, the elbow and arm below the shoulder joint. One surgical team will work on removing the hand from the donor as another team simultaneously prepares the arm on the recipient. Surgeons will then connect the donor hand's blood vessels to the patient's blood vessels under a microscope to restore blood circulation before connecting nerves and other tissue, such as bone, cartilage and muscles, as needed. Immediately after surgery, the hand transplant recipient will be taken to the Intensive Care Unit (ICU) for observation. The patient will typically stay in the ICU for one or two days and then be moved to a private room. At this point, a physical therapist will start working with the patient to rehabilitate the transplanted hand, and a psychiatrist will discuss any psychological concerns. The patient will stay in the hospital until both the plastic surgery and medical transplant teams agree that it is safe for the patient to return home. This post-operative stay is anticipated to be approximately 7-14 days, but can vary due to a number of factors. Rehabilitation with the physical therapist will take several hours a day while the hand transplant recipient is at the hospital. Following discharge from the hospital, hand transplant patients will need to return to BWH for routine visits. These visits will include monitoring transplant drug levels (immune suppressants) through regular blood tests, rehabilitative therapy, imaging tests, assessing quality of life, and checking for the return of sensation and movement to the hand. Rehabilitation visits will take place daily for several months, whereas the other visits will typically take place on a weekly basis for the first three months and then at least once a month for the first year following surgery. After the first year, it is expected that hand transplant patients will need to visit the hospital less frequently. However, patients must be prepared to make a lifetime commitment to immune suppressants to help prevent the rejection of the transplanted hand.
Criteria:   Inclusion Criteria: - Age between 18 and 60 years. - Single dominant hand or bilateral hand amputation. - Time elapsed since amputation more than 6 months but less than 15 years. - Patient has tried myoelectric prosthesis without success. - Level of amputation anywhere from the wrist joint to just below the shoulder joint, which should be functional. - Signed written informed consent. - Willing to complete psychological and social evaluations. - Willing to take immunosuppressants - drugs that help prevent rejection of the transplant - for life. - Willing to comply with extensive post-transplant rehabilitation for a minimum of two years. - Willing to return for follow-up visits as determined by the treating physician. - Willing to receive standard vaccinations prior to the transplant, such as influenza and hepatitis B. Exclusion Criteria: - Single, non-dominant hand amputees. - Active malignancy. - High risk of return of malignancy. - History of persistent non-compliance. - Findings of psychological evaluation that indicate inability to comply with physician's orders or mental instability. - Any diagnosis that puts the subject at risk from hand transplant surgery or life-long immune suppression. - Inability to ensure adequate follow-up of post-transplant care and immune suppression.
NCT ID:   NCT01293214
Primary Contact:   N/A
Backup Contact:   N/A
Location Contact:   Boston, Massachusetts 02115
United States

Lisa Quinn
Phone: 617-732-5303
Email: lquinn1@partners.org

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 19, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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