Shoulder Dislocation Clinical Trial
Official title:
BION Implantable Microstimulation System
The study looks at treatments for reversing chronic shoulder subluxation after a stroke. It compares electrical stimulation with surface electrodes (stimulation through the skin) with intra-muscular stimulation (from inside the muscle)using an implanted micro-stimulator (BION). Subjects are put either in a surface stimulation or a BION® group. In the BION® group, two BION®s are implanted in the shoulder, the medial deltoid and supraspinatus muscles. Treatment consists of a baseline of 6 weeks, and 6 weeks of therapy, consisting of 2 sessions per day for 10 to 30 minutes each time. This is followed by 6 weeks without therapy. If testing shows that after 6 weeks of therapy there is no reversal of subluxation, more intense therapy is carried out for another 6 weeks. Treatment is similar in the surface electrode group, but surface electrodes deliver the stimulation instead of BION®s. A total of 30 subjects is expected to complete the study.
The BION™ is a novel implantable neuromuscular stimulator whose intended use in this study
is to reanimate the shoulder muscles of stroke survivors with shoulder subluxation. Strokes
are considered to be the most important cause of adult disability in North America, with
500,000 new cases per year in the U.S. (National Stroke Association) and 45,000 in Canada
(Langton-Hewer, 1990; Shuaib & Hachinski, 1991). Three-quarters of these patients survive
and half of the survivors have substantial muscle weakness after 6 months (Gresham et al.,
1979) with little chance of spontaneous recovery (Anderson, 1990; Bonita & Beaglehole,
1988). The most commonly affected region in the early phases of recovery is the shoulder;
80% of hemiplegic stroke patients suffer from shoulder subluxation and associated chronic
pain (Smith et al., 1980). The shoulder muscles that are normally active tonically are
flaccidly paralyzed; the weight of the pendant arm gradually stretches and damages the
atrophic muscles and ligaments, allowing the head of the humerus to descend out of the
glenoid fossa. This results in chronic shoulder pain that is difficult to treat and tends to
obstruct physical therapy directed toward regaining some use of the paretic arm. Our
hypothesis is that electrical stimulation delivered by the BIONs should be fundamentally
equivalent to muscle activation achieved voluntarily or by transcutaneous electrical nerve
stimulation (TENS), but that the BIONs will prove to be a more clinically acceptable and
effective approach. The BION system consists of the BION implants themselves, a controller
that is operated by the study participant, and fitting hardware and software used by the
clinician to implant, test, and program BION function.
In this study, the BION will be used to reanimate the shoulder muscles of stroke survivors
experiencing shoulder subluxation. The objective of this study is to evaluate the safety and
efficacy of intramuscular stimulation of BIONs to correct established, symptomatic shoulder
subluxation in chronic stroke survivors. The results of intramuscular stimulation by BIONs
will be compared with the results of treatment with conventional therapy: surface
stimulation.
Degree of shoulder subluxation will be the primary outcome measure for the study. We have
included other (secondary) outcome measures (i.e., muscle strength, range of motion,
functional activity, spasticity/tone, subject satisfaction and pain) which may reveal
secondary benefits of treatment with BIONs. The investigation is expected to last up to 21
weeks for each study participant. The study will be completed over a 5-year period.
;
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Not yet recruiting |
NCT05635240 -
Chronic Anterior Shoulder Instability in the Military
|
||
Recruiting |
NCT02913352 -
Latarjet Versus Modified Eden-Hybinette for Anterior Shoulder Dislocation
|
N/A | |
Completed |
NCT03154957 -
Management of Acute Dislocation of Emergency in the University Hospital of Strasbourg Shoulder: Retrospective Evaluation of Practices and Proposal of a Clinical Path
|
||
Recruiting |
NCT02510625 -
The Arthroscopic Treatment of Recurrent Anterior Shoulder Instability
|
N/A | |
Completed |
NCT00707018 -
Immobilization in External Rotation After First Time Anterior Shoulder Dislocation
|
N/A | |
Recruiting |
NCT04887337 -
Early arthroscoPic Stabilization veRsus rehabilitatiOn of the Shoulder in Adolescents With a trauMatic First-time Anterior Shoulder Dislocation ePisode
|
N/A | |
Completed |
NCT04960137 -
Shoulder Dislocations Treated With Button Plates and Non-absorbable Suture Anchor
|
N/A | |
Recruiting |
NCT05388942 -
Virtual Reality Hypnosis Versus Inhaled Nitrous Oxide in Anterior Shoulder Dislocation Reduction: an Open Multicenter Randomized Controlled Trial
|
N/A | |
Completed |
NCT02725333 -
Does Shoulder Stabilizations Stabilize Shoulders?
|
N/A | |
Recruiting |
NCT05705479 -
Shoulder Instability Trial Comparing Arthroscopic Stabilization Benefits Compared With Latarjet Procedure Evaluation - STABLE Definitive Trial
|
N/A | |
Not yet recruiting |
NCT05048303 -
Multicenter Clinical Cohort Study of Modified Flexible Fixation Latarjet Procedure for Recurrent Shoulder Dislocation
|
N/A | |
Recruiting |
NCT03453710 -
Remplissage Versus Latarjet Coracoid Transfer for Recurrent Shoulder Instability
|
N/A | |
Recruiting |
NCT04952636 -
A Prospective Comparative Study of Arthroscopic and Open Surgery in Cuistow Procedure
|
N/A | |
Completed |
NCT00251264 -
Arthroscopic Versus Open Stabilization for Traumatic Shoulder Instability
|
N/A | |
Terminated |
NCT02426996 -
The Latarjet-type Procedure Using the SEM Positioner: Using a Scan to Assess Consolidation
|
N/A | |
Completed |
NCT04022629 -
ASSET 2 Study: Long-Term Follow-up of a Randomised Control Trial
|
Phase 2/Phase 3 | |
Terminated |
NCT04820491 -
Efficient Anterior Shoulder Ultrasound Reduction Multicenter Prospective Randomized Trial
|
N/A | |
Recruiting |
NCT05443295 -
Improvement of Fatigue in Unstable Shoulder Through a Therapeutic Exercise Program in Physiotherapy
|
N/A | |
Completed |
NCT06459258 -
Throwing Velocity and Patient Reported Outcomes in Elite Level Handball Players After Completion of Shoulder-Pacemaker Strength Training
|
N/A | |
Completed |
NCT04479397 -
Sling vs Nothing After Latarjet Procedure
|
N/A |