Purpose

The goal of this observational study is to determine if nerve transfer surgeries improve upper extremity function and quality of life in patients with a high level cervical spinal cord injury. Participants will: - undergo standard of care pre- and post-op testing and study exams - complete pre- and post-questionnaires - undergo standard of care nerve transfer surgeries - follow-up with surgeon at 6/12/18/24/36 and potentially at 48 months - attend therapy at local therapist for up to 2 years postop.

Conditions

Eligibility

Eligible Ages
Between 18 Years and 80 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • 18-80 years of age - High cervical SCI (motor level C1-C4) - Motor complete SCI AIS grade A-B - Plateaued spontaneous recovery for at least 6 months of non-operative therapy - SCI greater than 6 months and fewer than 60 months since injury - At least MRC 4/5 donor strength - Mentally and physically willing and able to comply with evaluations

Exclusion Criteria

  • Active infection at the operative site or systemic infection - Any return or ongoing recovery of distal motor function - Significant joint contractures and/or limitations in passive range of motion in the arm - Mentally or physically compromised making it impossible to complete study activities - Immunologically suppressed - Currently undergoing long-term steroid therapy - Active malignancy - Pregnancy

Study Design

Phase
Study Type
Observational
Observational Model
Case-Only
Time Perspective
Prospective

Recruiting Locations

Stanford University
Stanford, California 94305
Contact:
Anthony Bet
650-683-5823
abet0915@stanford.edu

University of Miami
Miami, Florida 33136
Contact:
George Jimsheleishvili, MD
305-243-4781
gxi150@med.miami.edu

Johns Hopkins University
Baltimore, Maryland 21287
Contact:
Chava Roberts
667-306-8862
crober83@jh.edu

University of Michigan
Ann Arbor, Michigan 48109
Contact:
Savannah Solomon
734-936-7010
ssavanna@med.umich.edu

Washington University in St. Louis
St Louis, Missouri 63110
Contact:
Linda Koester
13143627368
koesterl@wustl.edu

Wake Forest Medical Center
Winston-Salem, North Carolina 27157
Contact:
Wendy Jenkins
336-716-3842
wendy.jenkins@advocatehealth.org

University of Pennsylvania
Philadelphia, Pennsylvania 19104
Contact:
Leah Coghlan
215-341-5864
leah.coghlan@pennmedicine.upenn.edu

Houston Methodist
Houston, Texas 77030
Contact:
Amber Behne
346-238-6424
abehne@houstonmethodist.org

University of Utah
Salt Lake City, Utah 84132
Contact:
Kirstianna Lombardi
801-585-9821
kirstianna.lombardi@utah.edu

More Details

Status
Recruiting
Sponsor
Washington University School of Medicine

Study Contact

Linda Koester, BS
314-362-7368
koesterl@wustl.edu

Detailed Description

Restoration of function in patients with high tetraplegia has been an elusive clinical challenge. There is a critical need to find an effective reconstructive therapy/procedure which improves the upper extremity function in patients with high tetraplegia. One pure motor nerve - spinal accessory nerve (SAN) remains a viable donor in high tetraplegia patients to successfully restore elbow flexion or extension. Elbow function can provide profound independence in mobility, ventilator management and may broaden the application of assistive therapies. The two objectives of this study are: - Determine if SAN nerve transfer surgery can improve the reinnervation of bicep or tricep muscles in high tetraplegia patients. - Determine if SAN nerve transfer surgery can reanimate upper arm function and improve functional independence in patients with high tetraplegia. Study Activities (including standard of care (SOC)) - Electrodiagnosis pre-op (SOC) - Upper extremity maximum muscle testing (SOC) - Questionnaires (SOC and study-related (SR)) - Exams by a study therapist (SR) - Neurological exam - ISNCSCI - (SOC) - Nerve Transfer Surgery to be determined by surgeon (SOC) - Follow-up visits with surgeon at 6/12/18/24/36 and potentially 48 months - post-op electrodiagnostic testing (SR) - post-op upper extremity maximum muscle testing (SOC) - post-op questionnaires - post-op therapy exams (SR)

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.