Insufisciency of recruitment

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.

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.

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