Influence of an Anterior Latarjet-type Abutment Operation on Scapular Dyskinesia and the Muscular Stabilization Mechanisms of the Scapula (DyScapLat)
NCT ID: NCT05131126
Last Updated: 2021-11-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
50 participants
INTERVENTIONAL
2019-05-22
2023-05-22
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Patient requiring anterior abutment surgery by Latarjet method
Latarjet method
This operation consists of fixing a bone graft
Different arms exercices
Perform 5 elevation movements in each of the elevation planes (sagittal, scapular and coronal) with the right and left arms
* Perform 5 circumduction movements with the right and left arms
* Maintain a weight of 1kg twice for 5 seconds with the arms at 90 ° of elevation.
Healthy volunteers
Different arms exercices
Perform 5 elevation movements in each of the elevation planes (sagittal, scapular and coronal) with the right and left arms
* Perform 5 circumduction movements with the right and left arms
* Maintain a weight of 1kg twice for 5 seconds with the arms at 90 ° of elevation.
Interventions
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Latarjet method
This operation consists of fixing a bone graft
Different arms exercices
Perform 5 elevation movements in each of the elevation planes (sagittal, scapular and coronal) with the right and left arms
* Perform 5 circumduction movements with the right and left arms
* Maintain a weight of 1kg twice for 5 seconds with the arms at 90 ° of elevation.
Eligibility Criteria
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Inclusion Criteria
* Male between 18 and 40 years-old
* Practice a regular sports activity before the injury (s) requiring surgery
* Present the clinical criteria leading to anterior abutment surgery using the Latarjet method
* Surgery performed by surgeons from the Jean-Mermoz Private Hospital (69008 Lyon)
* Have followed a post-surgery self-rehabilitation program
Control group:
* Male between 18 and 40 years-old
* Practice a regular sports activity
Both group:
oPatient having signed an informed consent o Subject affiliated or beneficiary of a social security scheme
Exclusion Criteria
* Have another shoulder pathology on the side of the operated limb or on the contralateral side
* Present a constitutional hyper laxity
* Have stiffness or recurrence of dislocation of the shoulder post-surgery
* Have a body mass index greater than 30 kg / m² (to ensure sufficient accuracy to measure the movements of the scapula)
* Wear a pacemaker or any other metal device (e.g. patch with metal material)
* Present a contraindication to the use of measuring devices (intolerance to a weak electromagnetic field)
Control group:
* Present during the study or have presented in the past any musculoskeletal pathology in the right or left shoulder (WOSI or WORC score greater than 250).
* Have a body mass index greater than 30 kg / m² (to ensure sufficient accuracy to measure the movements of the scapula)
* Wear a pacemaker or any other metal device (e.g. patch with metal material)
* Present a contraindication to the use of measuring devices (intolerance to a weak electromagnetic field)
Both group :
o Protected subject: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision
18 Years
40 Years
MALE
Yes
Sponsors
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European Clinical Trial Experts Network
OTHER
Ramsay Générale de Santé
OTHER
Responsible Party
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Locations
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Hopital privé Jean Mermoz
Lyon, , France
Countries
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Central Contacts
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Facility Contacts
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Lionel Neyton, Dr
Role: primary
Other Identifiers
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2018-A02449-46
Identifier Type: -
Identifier Source: org_study_id