Preliminary Study of Feasibility of Arthrodesis Scapula-humeral Under Arthroscopy (DESEP)

Regional University Hospital Center (CHRU)

Status: Terminated

Conditions: Arthroscopy Arthrodesis Gleno-humeral

Treatments: Procedure: arthroscopy arthrodesis of the shoulder

Study type: Interventional

Funder types: Other

Identifiers

NCT02566382

RB 12.172 DESEP

Details and patient eligibility

About

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.

Full description

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.

Enrollment: 1 patient

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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1 participants in 1 patient group

shoulder arthroscopy arthrodesis

Experimental group

Description:

The shoulder surgery will be realized under arthroscopy only.

Treatment:

Procedure: arthroscopy arthrodesis of the shoulder