Tornier Blueprint Planning Software in Patients Receiving Reverse Shoulder Arthroplasty

Status unconfirmed · Not applicable

Conditions studied: Reverse Shoulder Replacement

In brief

Compare sizing determined in pre-operative planning of reverse shoulder arthroplasty to operative implant size selected.

Key facts

Study ID

NCT04474665

Run by

Spine Institute of Louisiana Foundation

People needed

20

Starts

2020-03-16

Expected to finish

2021-06-01

Last updated by the study team

2020-07-17

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Skeletally mature, and age ≥ 18 years.
• In the opinion of the treating surgeon, must already be a qualified candidate for reverse shoulder arthroplasty without the use of glenoid bone grafts.
• Be likely to return for regular follow-ups until the end of the study period.
• Be willing and able to provide Informed Consent for study participation.

You may not qualify if…

• Previous bony surgery on the operative shoulder.
• Shoulder pain due to acute trauma.
• Clinical, laboratory and/or radiological evidence of shoulder pain secondary to acute or chronic infection, malignancy, other space occupying lesions and metabolic bone demineralization diseases (e.g. osteomalacia, gout, Paget's disease etc.)
• Any active malignancy, infectious process, or documented chronic autoimmune disease.
• Any other concurrent medical disease or treatment that might impair normal healing process.
• Recent history (within past 6 months) of any chemical or alcohol dependence.
• Currently a prisoner.
• Currently experiencing a major mental illness (psychosis, schizophrenia, major affective disorder) which may indicate that the symptoms are psychological rather than of physical origin.
• Pregnant or planning to become pregnant within study duration.

Where it is running

• Spine Institute of Louisiana — Shreveport, Louisiana, United States

Full record on ClinicalTrials.gov

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