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Safety and Performance of JOURNEY™ II Cruciate Retaining (CR) Total Knee System (TKS) (JIICR)

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Smith & Nephew

Status

Completed

Conditions

Journey II CR Total Knee System

Treatments

Device: Total knee arthroplasty with Journey II CR Total Knee System

Study type

Observational

Funder types

Industry
Other

Identifiers

NCT03885531
2018.19.KNE.JIICR.RET

Details and patient eligibility

About

The objective of this study is to examine the safety and performance of the Journey II CR TKS based on retrospective data.

Enrollment

586 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subject received primary uni- or bilateral TKA with the Journey II CR TKS for an approved indication;
  • The TKA occurred at least 12 weeks prior to enrollment

Exclusion criteria

  • None

Trial contacts and locations

6

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Data sourced from clinicaltrials.gov

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