iTotal Pilot Study of ConforMIS Custom Total Knee Implant

Completed · Not applicable

Conditions studied: Knee Arthroplasty, Total

In brief

To compare the outcomes of patients receiving the ConforMIS custom total knee implant to the outcomes of patients who receiving an off-the-shelf total knee implant. Hypothesis: Patient-specific, custom total knee implants manufactured from patient CT data, and implanted with CT-navigated custom instruments will show faster functional recovery, including gait and patient functional outcome scores, when compared to standard, off-the-shelf total knee components inserted with non-navigated instruments (the present standard of care in total knee surgery).

Key facts

Study ID

NCT02186587

Run by

University of Missouri-Columbia

People needed

28

Starts

2014-06-01

Expected to finish

2016-04-01

Last updated by the study team

2023-05-23

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• undergoing total knee arthroplasty

You may not qualify if…

• BMI >40

Where it is running

• Missouri Orthopaedic Institute — Columbia, Missouri, United States

Full record on ClinicalTrials.gov

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