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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01204736
Other study ID # B7515-R
Secondary ID
Status Completed
Phase N/A
First received September 15, 2010
Last updated February 8, 2016
Start date August 2011
Est. completion date December 2015

Study information

Verified date February 2016
Source VA Office of Research and Development
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

Active elbow extension has significant functional benefits for individuals with tetraplegia. The proposed work will provide information to assess how effectively people are using their elbow extension tendon transfers, and whether one surgery works more effectively than the other. This study will provide recommendations to clinicians about the possibility of improving function after surgery using rehab techniques.


Description:

Voluntary control of elbow extension significantly improves functional abilities for individuals with tetraplegia. As a result, surgical reconstruction of elbow extension via tendon transfer is considered a fundamental intervention that benefits the patient, even if other tendon transfers aimed at improving hand function are never performed. Presently, there are two common tendon transfer surgeries used to restore elbow extension following spinal cord injury. These are the posterior deltoid to triceps transfer and the biceps to triceps transfer. Both surgeries significantly improve voluntary elbow extension, although there is variability in the amount of control that is restored among patients. This study will directly compare the performance of the posterior deltoid transfer to the biceps transfer with regard to: voluntary elbow extension strength, the ability to activate the transfer, and neural factors associated with voluntary and involuntary control of individual muscles. These comparisons will be made in functionally relevant postures and will provide fundamental information that will improve clinical understanding of the capacity of each of these two procedures to restore elbow extension.

The fundamental hypothesis of this proposal is that an inability to maximally activate the transferred posterior deltoid and the transferred biceps significantly limits the elbow extension moment that can be produced.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date December 2015
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Cervical Spinal Cord Injury (C5-C7)

- Posterior Deltoid to Triceps Tendon Transfer at least one year post-surgery

- Biceps to Triceps Tendon Transfer at least one year post-surgery

Exclusion Criteria:

- Subjects will be excluded from the studies if there is presence of concurrent severe medical illness, including:

- unhealed decubiti

- use of baclofen pumps

- existing infection

- cardiovascular disease

- significant osteoporosis (as indicated by a history of fractures following injury)

- or a history of pulmonary complications or autonomic dysreflexia

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Edward Hines Jr. VA Hospital, Hines, IL Hines Illinois

Sponsors (6)

Lead Sponsor Collaborator
VA Office of Research and Development Case Western Reserve University, Loyola University, MetroHealth System - Cleveland, OH, Northwestern University, Rehabilitation Institute of Chicago

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Elbow Extension Strength Elbow extension strength was measured as the maximum elbow extension moment that subject's could generate. We used an elbow moment transducer to measure elbow moments under isometric (no change in arm posture) conditions. Subjects performed three trials at maximum effort, holding maximum elbow extension for 5 to 7 seconds. The maximum moment was computed as the maximum average moment sustained over a 0.5 second window. At least one year post surgery No
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