Kettering, Ohio 45429

  • Osteoarthritis, Knee

Purpose:

This is a multi-centered prospective, consecutively enrolled study that will be conducted in the United States. Surgeons that are new users of the iTotal Knee system (defined by no experience using the customized Total Knee Replacement (TKR) in the last 6 months) will be involved in the study. To complete the study protocol, the center will collect baseline surgical and training data on 10 "off-the-shelf" TKR patients using the implant system the surgeon currently uses. Then the first 50 consecutive patients who have been identified to receive the iTotal implant (Cruciate-Retaining or Posterior-Stabilizing) based on patient factors and the implant system IFU will be enrolled in the study. Simultaneous bilateral Total Knee Arthroplasty cases will be excluded.


Criteria:

Inclusion Criteria: - > 18 years of age Exclusion Criteria: - Participation in another clinical study which would confound results - Inability to complete the protocol in the opinion of the clinical staff due to safety or other reasons - Simultaneous bilateral Total Knee Arthroplasty cases


NCT ID:

NCT04180423


Primary Contact:

Colleen Smith
Phone: 7813459049
Email: colleen.smith@conformis.com


Backup Contact:

Email: sumesh.zingde@conformis.com
Sumesh Zingde
Phone: 7813459103


Location Contact:

Kettering, Ohio 45429
United States

Matthew Hess, MD

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: November 27, 2022

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