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Five and Ten Year Results of the CMK21 Hip System

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Smith & Nephew

Status

Terminated

Conditions

Osteoarthritis

Treatments

Device: CMK21 Hip system

Study type

Observational

Funder types

Industry

Identifiers

NCT03908151
R11008-2B

Details and patient eligibility

About

Five and ten year results of the CMK21 Hip system

Full description

This study is being conducted to collect long term retrospective and prospective clinical and radiological data to evaluate the safety of revision rate and adverse events, and efficacy of clinical and patient assessment of the CMK21 hip stem in primary total hip arthroplasty.

Enrollment

100 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion:

  • The patients enrolled in the study were already operated at the time of the screening.
  • All the patients with osteoarthritis of the hip who received CMK21 hip stem between 2005 and 2007.
  • Skeletally mature patients requiring primary total hip arthroplasty due to non-inflammatory arthritis (degenerative joint disease) such as osteoarthritis, avascular necrosis, or traumatic arthritis.

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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