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Outcomes Study of the Trabecular Metal (TM) Reverse Shoulder System

← catalyst calendar

NCT01480440 · readout ≤ 134 d

Sponsored by Zimmer Biomet (industry) · ZBH — their whole pipeline →.

Phase
Status
Active, not recruiting
Study type
Observational
Enrollment
200estimated
Sites
5
Countries
United Kingdom, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
StartJan 2011actualWhen the study began enrolling
Primary completionDec 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionDec 2026estimatedThe whole study's end, after follow-up
First posted2011-11-28estimatedWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-28actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Osteoarthritis
  • Rheumatoid Arthritis
  • Post-traumatic Arthritis
  • Ununited Humeral Head Fracture
  • Irreducible 3-and 4-part Proximal Humeral Fractures
  • Avascular Necrosis
  • Gross Rotator Cuff Deficiency
  • Revision Total Shoulder Arthroplasty

Intervention

  • Device: Trabecular Metal Reverse Shoulder System — also filed as TM Reverse Shoulder System, TM Reverse System, TM Reverse

Primary outcome

what the primary-completion date above is the date OF
Survivorship
measured 10 Years

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