S.E.S Shoulder Arthroplasty Data Collection

• Register: ClinicalTrials.gov
• Last refreshed on: 16 December 2017
• Main ID: NCT00754416
• Date of registration: 16/09/2008
• Prospective Registration: No
• Primary sponsor: Zimmer Biomet
• Public title: S.E.S Shoulder Arthroplasty Data Collection
• Scientific title: A Prospective, Multicentre Study Evaluating the Clinical Performance of the S.E.S Shoulder Prosthesis
• Date of first enrolment: March 2003
• Target sample size: 100
• Recruitment status: Terminated
• URL: https://clinicaltrials.gov/show/NCT00754416
• Study type: Observational
• Phase: N/A

Countries of recruitment

Belgium, France

Contacts

• Name: Laurent BEGUIN, MD
• Affiliation: Centre hospitalier Bellevue

Key inclusion & exclusion criteria

Inclusion Criteria:

- A pre-operative level of pain and function the same as for conventional joint
replacement

- A likelihood of obtaining relief of pain and improved function

- Full skeletal maturity

- Ability to follow instructions

- Good general health for age

- Willing to return for follow-up evaluations

Exclusion Criteria:

- Glenohumeral joint infection, osteomyelitis

- Neuro-muscular complications

- Inability to co-operate with and complete the study



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

Health Condition(s) or Problem(s) studied

Arthritis

Primary Outcome(s)

Constance and oxford Scores [Time Frame: 6m, 1yr, 2yr, 3yr, 4yr and 5 yr]

Secondary Outcome(s)

Complication [Time Frame: Any time]

Patient Satisfaction [Time Frame: 6m,1yr,2yr,3yr,4yr and 5yr]

Secondary ID(s)

BMET FR 02

Source(s) of Monetary Support

Please refer to primary and secondary sponsors

Secondary Sponsor(s)

Biomet France SARL