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Preliminary Study of Feasibility of Arthrodesis Scapula-humeral Under Arthroscopy

NCT ID: NCT02566382

Last Updated: 2017-10-19

Study Results

Results pending

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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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

1 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-09-30

Study Completion Date

2017-10-31

Brief Summary

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Arthrodesis shoulder blade/humerus under arthroscopy. Implementation of an external fixative spray at the proximal level in the thorn of the scapula and distal in the diaphysis humerus.

Detailed Description

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This trial is about the arthrodesis shoulder blade/humerus under arthroscopy. The main aim of this study is to be able to carry out a fusion scapula-humeral supplements in 6 months. It is required to provide the benefice risk over to reduce the hospitalisation 48 hours.

Conditions

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Arthroscopy Arthrodesis Gleno-humeral

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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shoulder arthroscopy arthrodesis

The shoulder surgery will be realized under arthroscopy only.

Group Type EXPERIMENTAL

arthroscopy arthrodesis of the shoulder

Intervention Type PROCEDURE

The shoulder surgery will be realized under arthroscopy only

Interventions

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arthroscopy arthrodesis of the shoulder

The shoulder surgery will be realized under arthroscopy only

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patient having a deficit scapula-humeral mobility
* Impossibility of being operated for a preserving nervous surgery
* Patient affiliation with a social security
* Patient who signed inform consent

Exclusion Criteria

* Patient with No mobility in all the articulations of the shoulder
* Callus malunion of the higher end of the humerus or the glen of the scapula
* Unable to sign an inform consent
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Brest

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Brest university hospital

Brest, Brittany Region, France

Site Status

Countries

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France

Other Identifiers

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RB 12.172 DESEP

Identifier Type: -

Identifier Source: org_study_id