CompletedNot Applicable

Followup of Glenoid Fix Utilizing Auto Bone Graft in Shoulder Replacement

United States29 participantsStarted 2008-04-01

Plain-language summary

This is a case study to evaluate the adequacy of fixation and functional outcome of the glenoid anchor peg following autologous bone grafting around the prosthesis at the time of implant.

Who can participate

Age range19 Years – 90 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients who received a total shoulder replacement with an anchor peg glenoid and autologous bone grafting from the investigator of this study will be recruited for this study. Exclusion Criteria: * Patients will be excluded if they are unable to comprehend the consent information. * Pregnant women will be excluded from this study.

What they're measuring

Autologous bone graft, anchor-peg glenoid prosthesis and functional outcomes

Timeframe: case study over approximate 3 months time.

Trial details

NCT IDNCT00670852

SponsorUniversity of Nebraska

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2009-06-10

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