Nerve Transfers to Restore Hand Function in Spinal Cord Injury

Sponsor
Ottawa Hospital Research Institute (Other)
Overall Status
Withdrawn
CT.gov ID
NCT02861612
Collaborator
Ontario Neurotrauma Foundation (Other), Canadian Society of Plastic Surgeons (Other), Washington University School of Medicine (Other), Rick Hansen Institute (Other)
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Study Details

Study Description

Brief Summary

This study seeks to evaluate the efficacy of nerve transfers in restoring hand function in patients with cervical spinal injuries.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Nerve Transfer Surgery

Detailed Description

Cervical spinal cord injury is a life-altering injury that results in profound loss of upper limb function. Hand function is essential to basic activities of daily living and consequently has a significant impact on patients' quality of life. Tendon transfers and/or tenodesis have traditionally been used to restore hand function in spinal cord injuries - however, in recent years there is growing interest in the role of nerve transfers as a means of accomplishing this goal. Although preliminary results indicate nerve transfers may be well-suited for patients with spinal cord injury, their long term efficacy has not been demonstrated.

This study seeks to evaluate the efficacy of nerve transfers in restoring hand function in patients with cervical spinal injuries. Eligible patients will receive nerve transfer procedure(s) (e.g. brachialis to anterior interosseous nerve, supinator to posterior interosseous) and will be followed post-operatively to assess for changes in strength, functional independence, and quality of life.

Study Design

Study Type:
Observational
Actual Enrollment :
0 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Nerve Transfers to Restore Hand Function in Spinal Cord Injury
Study Start Date :
Aug 1, 2016
Anticipated Primary Completion Date :
Mar 18, 2019
Actual Study Completion Date :
Mar 18, 2019

Arms and Interventions

Arm Intervention/Treatment
Nerve Transfer

This is an observational study that looks at function and quality of life in patients before and after nerve transfer surgery.

Procedure: Nerve Transfer Surgery
Unilateral surgery will be performed under general non-paralytic anesthesia and no-tourniquet conditions to allow for responsive nerve simulation.

Outcome Measures

Primary Outcome Measures

  1. Upper extremity function - Myometric measures of strength (donor and recipient muscle groups) [Change from baseline at 6, 12, 24, 30 and 36 months post-surgery]

    Valid and reliable quantitative muscle strength measurement

  2. Upper extremity function - Manual muscle testing (MRC) [Change from baseline at 6, 12, 24, 30 and 36 months post-surgery]

    Quantitative assessment of motor function (MRC)

  3. Upper extremity function - Graded Redefined Assessment of Strength, Sensibility and Prehension test (GRASSP) [Change from baseline at 6, 12, 24, 30 and 36 months post-surgery]

    Valid, reliable and responsive measure of sensorimotor upper limb impairment specifically designed for patients with cervical SCI

  4. Upper extremity function - Range of motion [Change from baseline at 6, 12, 24, 30 and 36 months post-surgery]

    Quantitative assessment of range of motion (degrees)

Secondary Outcome Measures

  1. Health related quality of life - The Short Form (SF)-36 [Change from baseline at 6, 12, 24, 30 and 36 months post-surgery]

    Valid and responsive measure of quality of life in surgical patients

  2. Health related quality of life - Spinal Cord Independence Measure (SCIM I) [Change from baseline at 6, 12, 24, 30 and 36 months post-surgery]

    Disability scale developed to specifically address the ability of SCI patients to perform basic activities of daily living independently

  3. Health related quality of life - Canadian Occupational Performance Measure (COPM) [Change from baseline at 6, 12, 24, 30 and 36 months post-surgery]

    Evidence-based outcome measure designed to capture a patient's self-perception of performance in everyday living

  4. Health related quality of life - Semi-structured interviews [Collected at 12 and 24 months post-surgery.]

    Semi-structured interviews to gain information about satisfaction, acceptability, and the subjective experience of the surgical intervention, therapy, and functional outcome

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with a spinal cord injury AIS level C5 to C7. Those with motor complete injuries (AIS A or B) will be considered for surgical intervention if they are ≥ 5 months post injury. Motor incomplete patients (AIS C or D) will be considered if they are ≥ 1.5 years post injury.

  • Patients will require ≥ MRC 4 strength of the muscle supplied by the donor nerve (e.g. brachialis, supinator).

  • Finger flexor and extensor strength should be ≤ MRC 1 strength.

  • Muscles supplied by the donor nerve, will need to have no or minimal of evidence of lower motor neuron injury as dictated by evidence of fibrillations, positive sharp waves, or moderate or severely decreased recruitment on needle electromyography.

  • Those being evaluated for surgery outside nine-months post injury recipient muscles will be required to be free of lower motor neuron pathology.

  • Ability to comply and participate in rigorous post-surgical therapy regimen.

Exclusion Criteria:
  • Comorbidities precluding safe surgery including autonomic/hemodynamic instability, pulmonary instability, active infection, chronic pressure sores or untreated urinary tract infections as determined by physician.

  • Simultaneous tendon transfer or tenodesis surgery (which would preclude separation of the effect of nerve transfer alone).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Washington University School of Medicine Saint Louis Missouri United States 63110
2 The Ottawa Hospital Ottawa Ontario Canada K1Y 4E9

Sponsors and Collaborators

  • Ottawa Hospital Research Institute
  • Ontario Neurotrauma Foundation
  • Canadian Society of Plastic Surgeons
  • Washington University School of Medicine
  • Rick Hansen Institute

Investigators

  • Principal Investigator: Kirsty U Boyd, MD, The Ottawa Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Ottawa Hospital Research Institute
ClinicalTrials.gov Identifier:
NCT02861612
Other Study ID Numbers:
  • 5313
First Posted:
Aug 10, 2016
Last Update Posted:
Mar 21, 2019
Last Verified:
Mar 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Ottawa Hospital Research Institute
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 21, 2019