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Discovery Elbow Long-Term Survivorship

Zimmer Biomet logo

Zimmer Biomet

Status

Terminated

Conditions

Survivorship
Pain

Treatments

Device: Discovery elbow minimally constrained

Study type

Observational

Funder types

Industry

Identifiers

NCT01308463
ORTHO.CR.EX002

Details and patient eligibility

About

The Discovery™ Elbow Multi-Center Prospective Study (5-year Study) patients will be consented at the two year or next scheduled follow-up period for the early-enrolled patients.

Full description

Eligibility: Patient(s) must be enrolled in the Discovery Multi-Center Prospective Study. The patient must consent to participation in the Discovery Long-term Survivorship Study.

In order to continue to follow the multi-center subjects long-term Biomet would like to extend the follow-up to include annual follow-ups from 10 to 15 years to document long-term survivorship. The annual follow-up will be obtained by sending annual questionnaire directly to the patients by mail. The Patient ASES questionnaire and survivorship data questions will be collected.

Enrollment

29 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Participant in the Discovery Elbow Multi-center Study
  2. Consent to participate in the Discovery Elbow Long-Term Survivorship Study

Exclusion criteria

  1. Patient is not a Discovery Elbow Multi-center Participant
  2. Patient does not provide consent for the Discovery Elbow Long-term Survivorship Study

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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