Preliminary Study of Feasibility of Arthrodesis Scapula-humeral Under Arthroscopy

• Register: ClinicalTrials.gov
• Last refreshed on: 16 December 2017
• Main ID: NCT02566382
• Date of registration: 29/09/2015
• Prospective Registration: No
• Primary sponsor: University Hospital, Brest
• Public title: Preliminary Study of Feasibility of Arthrodesis Scapula-humeral Under Arthroscopy DESEP
• Scientific title: Arthrodesis Gleno Humeral Under Arthroscopy in the Sequelae of Plexus Brachial Evaluation of the Technical Feasibility
• Date of first enrolment: September 2015
• Target sample size: 1
• Recruitment status: Terminated
• URL: https://clinicaltrials.gov/show/NCT02566382
• Study type: Interventional
• Study design: Intervention model: Single Group Assignment. Primary purpose: Treatment. Masking: None (Open Label).
• Phase: N/A

Countries of recruitment

France

Key inclusion & exclusion criteria

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



Age minimum: 18 Years
Age maximum: N/A
Gender: All

Health Condition(s) or Problem(s) studied

Arthroscopy Arthrodesis Gleno-humeral

Intervention(s)

Procedure: arthroscopy arthrodesis of the shoulder

Primary Outcome(s)

Radiological fusion gleno humeral on side and front view after the 6th month of the arthroscopy interventional [Time Frame: 6 months]

Secondary Outcome(s)

Blood loss [Time Frame: 3 days]

Secondary ID(s)

RB 12.172 DESEP

Source(s) of Monetary Support

Please refer to primary and secondary sponsors